Archive for March 2nd, 2008

‘2-Faced’ Particles Act Like Tiny Submarines

Sunday, March 2nd, 2008

For the first time, researchers at North Carolina State University have demonstrated that microscopic “two-faced” spheres whose halves are physically or chemically different - so-called Janus particles - will move like stealthy submarines when one alternating electrical field is applied to liquid surrounding the particles.

A paper describing the research, published in the Feb. 8, 2008, edition of Physical Review Letters, advances knowledge about how potential “smart” materials - think of minikin engines or sensors - can move around and respond to changes in their environment. Janus particles could be used as microscopic mixers, molecular “shuttles,” self-propelling microsensors or means of targeted drug giving.

The researchers - Dr. Orlin Velev, associate professor of chemical and biomolecular engineering at NC State and lead author of the paper; Sumit Gangwal, an NC State graduate student; Dr. Olivier Cayre, a post-doctoral researcher in Velev’s lab; and Dr. Martin Bazant from Massachusetts Institute of Technology - created tiny two-faced gold and plastic particles and applied low frequent occurrence alternating current to the water containing the particles. The electric field was of voltage and frequency similar to the ones you’d get if you plugged a device into a socket in your home or office.

Velev says the micrometer-sized particles convert the electrical field into liquid motion around them and then unexpectedly propel themselves perpendicular to the direction of the powered electrodes - not in the direction of the electrical field, as would be expected. The particles always travel in the same orientation: with the plastic “face” as the front of the mini-submarine and the metallic “face” in the rear, Velev added.

The phenomenon - called “induced-charge electrophoresis,” which had been predicted in a theoretical model by the MIT collaborator - had not been demonstrated previously.

The term “Janus particle” comes from the name of a Roman providence with two faces. Velev says that these materials have the potential to perform a variety of applications.

“You can imagine other types of Janus particles comprising a ’smart gel‘ that responds to a change in its environment and for this reason releases drugs, for example,” Velev says. Fabricating these responsive materials on the microscale and nanoscale is an exciting and rapidly developing area of science, he adds.

“We are able to create tiny Janus particles of the same size and shape and are beginning to learn how to give them functionality,” Velev said. “The next step is to appoint more complex particles that are able to perform more specialized functions in addition to propelling themselves around.”

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Article adapted by Medical News Today from original press release.
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The research is funded by the National Science Foundation and a Camile and Henry Dreyfus Teacher-Scholar grant.

The abstract of the paper follows.

“Induced Charge Electrophoresis of Metallodielectric Particles”
Authors: Sumit Gangwal, Olivier J. Cayre and Dr. Orlin D. Velev, NC State University; Dr. Martin Z. Bazant, Massachusetts Institute of Technology
Published: Feb. 4, 2008, in Physical Review Letters

Abstract: The application of ac electric fields in aqueous suspensions of anisotropic particles leads to unbalanced liquid flows and nonlinear, induced-charge electrophoretic motion. We relate experimental observations of the motion of Janus microparticles with one dielectric and one metal-coated hemisphere induced by uniform fields of frequency 100Hz-10kHz in NaCl solutions. The motion is perpendicular to the field axis and persists after particles are attracted to a glass wall. This phenomenon may find application in microactuators, microsensors and microfluidic devices.

Source: Dr. Orlin Velev
North Carolina State University

Real Time Imaging Device May Improve Surgery For Congenital Colon Disease

Sunday, March 2nd, 2008

Researchers at Cedars-Sinai Medical Center are developing a spectral imaging system that could consequence in shorter operating times beneficial to infants undergoing surgery for Hirschsprung’s disease, according to a mouse study reported in the Journal of Biophotonics

The study documents that in addition to its diagnostic potential, spectral imaging may provide an “optical biopsy,” allowing precise localization of a needed intervention.

Spectral imaging is based on the fact that light reflected from a target can be captured and measured by extremely sensitive equipment to develop a characteristic “signature” based on wavelength. In this study, the colon tissue of six mice with the tantamount of Hirschsprung’s disease was analyzed and compared to that of controls. through repeated measurements and calculations, unique signatures for normal tissue and for diseased tissue emerged.

Spectral imaging does not detect the neighborhood or inattention of ganglion cells themselves. Instead, the spectral signature reflects differences in the constitution of normal and diseased tissue.

As a result of this study in laboratory mice, human clinical trials will be planned, providing spectral imaging for intraoperative decision-making in Hirschsprung’s disease, a congenital condition affecting nerve cells of the large intestine. The technology, developed at Cedars-Sinai’s Minimally Invasive Surgical Technologies Institute (MISTI) is adaptable to other types of surgery.

Hirschsprung’s usually affects specialized nerve (ganglion) cells in the lower portion of the large intestine, although the entire colon can be involved. Ganglion cells normally stimulate smooth muscle of the intestinal wall to push stool through the colon, but in sections where ganglia are missing (aganglionosis) the process comes to a halt, causing severe constipation that can lead to obstruction, massive infection and even death.

Estimated to affect one in 5,000 babies, the disease can be treated in a minimally invasive surgical procedure that removes the diseased portion of the colon and attaches the bracing colon to the anus. One of the critical portions of the operation is the accurate and precise determination of the dot at which normal colon ends and disease begins. If too little colon is removed, the patient is likable to continue to cause to grow significant constipation, but if too much is removed, chronic diarrhea may result, which can lead to other major health problems.

“The location and length of the transition surface bounded by parallel circles between healthy and abnormal tissue varies considerably in Hirschsprung’s disease patients and be required to be precisely identified to properly perform the operation,” said Philip K. Frykman, M.D., Ph.D., Associate Director of Pediatric Surgery at Cedars Sinai and first author of the article. “The determination is routinely done by taking a number of small samples from the colon wall and sending them to the lab where a pathologist looks for the presence or absence of ganglion cells and other features. But this process may take 45 to 60 minutes, during which the operation is essentially on grasp and the patient remains under general anesthesia.

“Spectral imaging, on the other hand, could provide immediate results, increasing patient safety and operating room efficiency,” added Frykman, who specializes in minimally invasive surgery for infants and children and holds a research grant from Cedars-Sinai to study Hirschsprung’s disease.

There is a financial constituent, too. Reducing time in the operating room could make a misunderstanding of several thousand dollars.

“The images showed a clear distinction, and this was confirmed by pathological analysis. Based on our results, it appears that spectral imaging methods could be used during operations, in substantive time, to help surgeons distinguish normal from irregular tissue, without requiring traditional biopsy,” before-mentioned Daniel L. Farkas, Ph.D., vice-chairman for research in the Department of Surgery, director of the Minimally Invasive Surgical Technologies Institute, and senior author of the journal article.

Biophotonics the interdisciplinary field dealing with interactions between biological entities and photons, basic units of light is an emerging research area, with translational possible. Although spectral imaging and other photonic technologies have been used in advanced applications such as satellite reconnaissance for many years, only very freshly have scientists begun translating these approaches into biological and medical uses.

At Cedars-Sinai and a few biophotonic research centers in the United States and Europe, spectral imaging is being studied for possible use in a variety of surgical situations. For each potential application, newly developed devices, software and criteria are evaluated in animal studies to show “proof of concept” before human clinical trials are launched.

The Journal of Biophotonics is a strange, international literary production covering the broad range of research on the interaction between light and biological vital.

The study was supported in part by the US Navy Bureau of Medicine and Surgery.

Citation: Journal of Biophotonics, “Spectral imaging for precise surgical intervention in Hirschsprung’s Disease,” published online Feb. 25, 2008.

Cedars-Sinai Medical Center
8700 Beverly Blvd., Rm 2429A
Los Angeles, CA 90048
United States
http://www.cedars-sinai.edu

Beyond The Abstract: Female Sexual Dysfunction: A New Urogynaecological Research Field

Sunday, March 2nd, 2008

UroToday.com - Female sexual dysfunction represents a new and underestimated field in urogynaecological research.

Therefore, we provided an overview of the current literature to emphasize the growing importance and relevance of this widespread problem. In addition, it was the design to provide evidence that definitions, prevalence, diagnostic protocols and therapeutic possibilities are confusing and not standardized. Considering the importance of this problem, we tried to find out if it would be possible to answer some major questions: What is the “true” prevalence? What are the “standard” questionnaires? What are the causes and “profitable” therapies? Until now the scientific literature is too inadequate to provide even most basic data for diagnosis and treatment. The number of papers investigating this passage out is very scarce, and so far no randomized clinical trials have been performed. Furthermore, the most of the studies do not exercise standardized methods to assess this condition, and contrary to erectile dysfunction in men- sexual dysfunction is not defined as a disease in women. The use of standardized diagnostic tools is essential to determine the true prevalence and also the jeopardize factors of this condition. Appropriate treatment will be developed only if diagnosis is improved and if doctors pay appropriate attention to this medical problem that affects a high percentage of women.

Written Orietta Dalpiaz MD, FEBU as part of Beyond the Abstract forward UroToday.com. This initiative offers a method of publishing for the professional urology community. Authors are given an opportunity to expand on the circumstances, limitations, etc., of their research by referencing the published abstract.

Link to Full Abstract

UroToday - the only urology website with original content written by global urology key opinion leaders actively engaged in clinical practice.

To access the latest urology news releases from UroToday, go to: www.urotoday.com

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Reproduced on this account that Medical News Today with permission of UroToday.
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Atypical Protein Kinase C Stabilizes SRC-3 Levels In Breast Cancer Cells

Sunday, March 2nd, 2008

A new study provides valuable insight into a previously undescribed mechanism that regulates a prominent cancer-associated protein. The research, published by Cell Press in the February 29th issue of Molecular Cell, will enhance understanding of the principal processes that contribute to breast cancer.

It is well established that steroid receptor coactivator-3 (SRC-3/AIB1) plays key roles in cell growth, reproduction, metabolism and cytokine signaling, is overexpressed in many cancers and is a major player in tumorigenesis and cancer progression. It is also clear that protein kinases are often overactive in cancers and that distinct patterns of phosphorylation, induced by different signals and different kinases, can play a major role in regulating cancer-associated proteins, including SRC-3.

“Recently, it was shown that phosphorylation of SRC-3 by specific kinases is associated with increased degradation of SRC-3. However, kinases that stabilize SRC-3 in cancer cells have not to this time been reported,” explains take the lead of author Dr. Bert O’Malley from the Baylor College of Medicine. Dr. O’Malley and colleagues examined the interaction between atypical protein kinase C (aPKC), which is overexpressed in many cancers, and SRC-3.

The researchers found that aPKC stabilized cellular SRC-3 protein levels by inducing phosphorylation of a particular region of SRC-3. Specifically, phosphorylation of C-terminal residues induced a conformational change that made SRC-3 greater amount of resistant to degradation by the core proteasome. This effect of aPKC required estrogen and estrogen receptor and was not supported by other steroid receptors, suggesting that aPKC-mediated SRC-3 stabilization is a receptor-selective event. These results reveal a mechanism that links aPKC through estrogen-dependent germination and tumorigenesis and provide yet another layer of control for regulating levels of the SRC-3 oncogenic protein.

“Our data describe a new regulatory mechanism for SRC-3 protein turnover which may play one important role in regulating SRC-3 levels in normal and oncogenic cell growth,” offers Dr. O’Malley. “We propose that when aPKC is overexpressed in cancer cells, the consequence is increased SRC-3 function and powerful enhancement of estrogen-receptor target gene transcription and promotion of estrogen-dependent cell growth in cancer cells such as breast.”

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Article adapted by dint of. Medical News Today from original press release.
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The researchers include Ping Yi, Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX; Qin Feng, Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX; Larbi Amazit, Inserm, U693, Le Kremlin-Bicetre, France; David M. Lonard, Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX; Sophia Y. Tsai,Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX ; Ming-Jer Tsai, Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX; and Bert W. O’Malley, Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX .

Source: Cathleen Genova
Cell Press

Yissum Announces The Discovery Of A Novel Small Molecule With Potent Anti-Metastatic Activity

Sunday, March 2nd, 2008

Yissum Ltd., the Technology Transfer Company of the Hebrew University of Jerusalem, today announced that scientists from the School of Pharmacy at the Hebrew University of Jerusalem discovered a novel orally make use of drug that prevents metastasis formation in various types of cancers. The novel drug is a small molecule named cis-ACCP, which is a prototype of a family of compounds that may be administered vocally and was shown as highly effective in rodents free from inducing at all adverse side-effects. The development of the drug was a collaborative effort of the laboratories of Prof. Eli Breuer, Prof. Reuven Reich and Prof. Amnon Hoffman, all from the School of Pharmacy at the Hebrew University of Jerusalem. The work was published in the Journal of Medicinal Chemistry (Hoffman et al., electronic publication ahead of print: DOI: 10.1021/jm701087n).

Nava Swersky Sofer, Yissum’s President and CEO, stated, “This reinvigorated class of drugs could potentially change the lives of millions of cancer patients by providing protection from metastasis in the form of a pill. Of course, multiplied years of testing are ahead of us before the drug can reach the patients, but this is the first step.”

cis-ACCP, the novel drug, inhibits enzymes called matrix metalloproteinases (MMPs), which are extracellular enzymes known to gambler a crucial role in physiological tissue remodeling and repair. However, pathological over-expression of MMPs has been associated with a variety of chronic diseases including cancer, arthritis, osteoporosis, multiple sclerosis, arteriosclerosis, congestive heart failure, chronic obstructive pulmonary disease, liver cirrhosis, and others. In cancer, over-expression of MMPs enables the tumorigenic cells to invade other tissues, leading to metastasis composition. In most cases, this is a turning point that renders the tumor untreatable by conventional treatments.

The efficient inhibition of MMPs is therefore an important curative target that has attracted considerable attention within the research community for the last two decades. Yet, in spite of the huge effort devoted to this goal, no clinically useful inhibitor has been developed to date. The main obstacles encountered by scientists trying to develop such inhibitors were high toxicity leading to unacceptable side-effects, and low bioavailability since most of the potential drugs were not soluble in water and hence could not effectively reach the extracellular fluid, where their target proteins are found.

In contrast, cis-ACCP, has a very low toxicity as revealed by preclinical trials on rodents. This is achieved via two important properties of the drug: it inhibits the activity of selected MMPs without inhibiting similar proteins; and due to its hydrophilic (water-soluble) nature, the drug does not enter the cells, but rather stays in the extracellular fluid, where it exerts its effect. In other words, cis-ACCP is self-targeted to its allot site of action, namely outside cells, which reduces potential intracellular toxicities.

The preclinical experiments described in the paper also showed that the novel drug prevents cancer cells from invading adjacent tissues (and thus forming metastases), and is effective in treating melanoma (skin cancer) and prostate cancer in rodent model systems. The results showed that cis-ACCP significantly inhibited both tumor growth and metastasis formation.

About the Researchers

Professor Eli Breuer received his academic training at the Hebrew University of Jerusalem and his speed doctoral training in the laboratory of Nobel Laureate Herbert C. Brown at Purdue University in Lafayette, Indiana, USA. In the past he served as head strong of Department of Medicinal Chemistry and later as Director of School of Pharmacy of the Hebrew University of Jerusalem. Breuer was National Representative of Israel in the Division of Chemistry and Human Health of the International Union of Pure & Applied Chemistry (IUPAC) in spite of several years, and is currently a part of the Subcommittee on Medicinal Chemistry and Drug Development of IUPAC.

Professor Amnon Hoffman has transversely 20 years of experience in the field of pharmacokinetics and pharmacodynamics, with a special concern in the biological aspects of drug delivery systems. Prof. Hoffman is currently the Chairman of the Department of Pharmaceutics and Head of the MSc program in Clinical Pharmacy at The Hebrew University of Jerusalem’s School of Pharmacy. He has published over 100 scientific papers and book chapters. He holds 15 patents on novel drug delivery systems, and orally bioavailable peptides. In addition, he is the scientific co-founder of Intec Pharma, a startup company developing a recent technology sustained release drug delivery systems, Gastro-retentive Dosage Form (GDRF).

Professor Reuven Reich received his academic education at the Weizmann Institute of Science, Rehovot and his post doctoral training in the laboratory of Dr. George Martin at National institute of dental Research, NIH, Bethesda, USA. Professor Reuven Reich has over 20 years of experience in the field of metastasis research and metalloproteinases.

About Yissum

Yissum was founded in 1964 to protect the Hebrew University’s intellectual property and commercialise it. $1 Billion in annual sales are generated by products based on Hebrew University technologies licensed not at home by Yissum. Ranked among the top technology transfer companies in the world, Yissum has registered 5500 patents covering 1600 inventions; licensed out 480 technologies and spun out 65 companies.

Yissum’s business partners span the globe and include companies such as Novartis, Microsoft, Johnson & Johnson, Merck, Intel, Teva and many more. For further intelligence please visit http://www.yissum.co.il.

MIT Student Invents Knock-Out Punch For Antibiotic Resistance

Sunday, March 2nd, 2008

MIT graduate student and synthetic biologist Timothy Lu is passionate about tackling problems that pose threats to human soundness. His current mission: to destroy antibiotic-resistant bacteria.

The 27-year-old M.D. candidate and Ph.D. in the Harvard-MIT Division of Health Sciences and Technology received the prestigious $30,000 Lemelson-MIT Student Prize for inventing processes that promise to combat bacterial infections by enhancing the effectiveness of antibiotics at killing bacteria and helping to eradicate biofilm - bacterial layers that resist antimicrobial treatment and breed on surfaces, such as those of medical, industrial and food processing apparatus.

Bacterial infections can lead to censorious health issues. The Centers for Disease Control and Prevention estimates that the antibiotic-resistant bacterium MRSA, or methicillin-resistant Staphylococcus aureus, causes approximately 94,000 infections and contributes to 19,000 deaths annually in the United States, through contact that can occur in a variety of locations, including schools, hospitals and homes. Bacteria can also infect food, including spinach and beef, and damage industrial equipment.

Lu explained that fewer pharmaceutical companies are inventing new antibiotics due to lengthy exhibition epochs, high failure rates and large costs. According to the Tufts Center for the Study of Drug Development, the cost to develop a new drug is $930 million (based on the value of the dollar in 2006). These factors, coupled with a decline in the number of prescriptions authorized for antibiotics, constrain profits. “Antibiotic-resistant bacteria are also becoming more prevalent,” Lu noted. “My inventions enable the rapid design and production of inexpensive antibacterial agents that can break through the defenses of antibiotic-resistant bacteria and bacterial biofilms.”

Delivering a One-Two Punch

Working with his advisor, J.J. Collins, professor of biomedical engineering at Boston University, Lu developed two bacteriophage platforms to overcome antibiotic resistance. Bacteriophage are viruses that only infect bacteria, not human cells. They have been used since the timely 20th century to treat bacterial infections; however, they fell out of favor in the United States due to the advent of antibiotics. Lu’s work represents an exciting application of synthetic biology, which is an emerging field focused on the rational engineering of organisms to achieve novel functions.

Lu has engineered bacteriophage to boost antibiotic effectiveness. The bacteriophage carries DNA that codes for factors that target bacterial gene networks, what one. former treatments failed to reach, and destroys bacterial antibiotic resistance mechanisms. The weakened bacterial defenses enable antibiotics to perform better. Administered together, Lu’s bacteriophage and antibiotics have the potential to eliminate nearly 30,000 times more bacteria than antibiotics alone, including cells that survive antibiotic-only treatment. This combination treatment also thwarts development of stronger antibiotic resistance, which can extend the lifetime of existing and future antibiotic drugs.

“While working at a hospital as part of a graduate course, I adage many patients who contracted new infections due to already-compromised immune systems or equipment that is extremely difficult to keep sterile,” Lu recalled. “Being infected by difficult-to-eradicate bacteria is a traumatic experience for patients and a serious public health issue that needs attention. I thought that there had to exist a solution for these infections.”

Penetrating Biofilms

Lu also applied his work through bacteriophage to create a new technique for reducing baneful biofilms, which are slimy layers of bacteria that develop on the surfaces of sanatory, industrial and food processing equipment and are difficult to penetrate and remove. Current treatment methods to penetrate biofilms can involve peptides or enzymes, which must subsist administered systemically and are rich. Medical devices infected by biofilms, such as replacement hip joints or pacemakers, often have to be removed surgically.

Lu invented enzymatically-active bacteriophage that directly mark the infection site, where they can simultaneously penetrate the biofilm’s protective slime layer and slay the bacteria underneath. “Think of it as a Trojan Horse,” he explained. “First you sneak into the bacteria and use it to overproduce enzymes precisely where they are needed most in order to overwhelm and break up the biofilm slime. Once the slime is disrupted, the bacteriophage then move in and kill the bacteria.”

“As a physician who has treated patients with resistant bacterial infections, I am well aware of the devastating effect they acquire on morbidity and number of deaths,” added Collin M. Stultz, associate professor of biomedical engineering in the Harvard-MIT Division of Health Sciences and Technology, and one of Lu’s recommenders for the award. “Tim has developed a series of methods that can subsist used to treat such problematic infections.”

In tests, Lu’s platform proved greater than 99.997 percent effective at destroying biofilms - a significant improvement over current treatment options. “The ultimate goal is to develop a sustainable source of antibacterial therapies that are effective and easy to produce at low cost, and will extreme us through the 21st hundred,” said Lu.

According to Lu, his engineered enzymatically-active bacteriophage could be initially applied in food processing settings to kill food-borne bacteria, such as Escherichia coli (E. coli) that contaminate spinach and consideration severe illness when ingested. In line with these hopes, there is evidence that U.S. regulatory authorities are warming up to the therapeutic use of bacteriophage. For example, in 2006, the U.S. Food and Drug Administration approved the chief U.S. manipulation for Listeria pollution of processed meats using natural bacteriophage.

Lu added that enzymatically-active bacteriophage could also benefit industry by being used to treat infected pipes and reduce corrosion.

Inherited Inventiveness

Born in Stanford, California, and raised in Yorktown Heights, New York, and Taiwan, Lu credits his inventiveness to his father, Nicky, an engineer and entrepreneur who helped develop modern semiconductor memories with IBM and the integrated circuits industry in Taiwan. Lu recalls spending time at his father’s customary duty during his formative years, where he reviewed plans and designs for new integrated circuits.

“I inherited my interest in invention and entrepreneurship from my endow or supply with a father,” Lu said. “It was very inspiring to see the amount of effort my father and his team put into their work and their joy and elation when they achieved success.”

“Tim is one of the young stars in the emerging field of synthetic biology” said his advisor Collins. “I am confident he will be developed into a leading clinical investigator and innovator.”

“Tim demonstrates the type of eager for superiority and inventive thinking the $30,000 Lemelson-MIT Student Prize was established to recognize,” said Josh Schuler, executive director of the Lemelson-MIT Program, what one. provides the annual award. “What is truly impressive about Tim’s approaches is the breadth of his applications. Not only does his work have potential in healthcare, but also in protecting the general public through safer food processing and prevention of industrial biofouling. Harmful bacteria everywhere should be afraid.”

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Article adapted by Medical News Today from original press release.
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Second Year of National Student Prize Expansion

On February 28, the winners of the second annual $30,000 Lemelson-Illinois Student Prize and Lemelson-Rensselaer Student Prize will be announced at the University of Illinois at Urbana-Champaign and Rensselaer Polytechnic Institute, respectively. Details about each winner will be posted on http://www.30kprize.uiuc.edu/ and http://www.rpi.edu/lemelson/.

ABOUT THE $30,000 LEMELSON-MIT STUDENT PRIZE

The $30,000 Lemelson-MIT Student Prize is awarded annually to an MIT senior or graduate student who has created or improved a product or process, applied a technology in a new way, redesigned a system, or demonstrated remarkable inventiveness in other ways. A distinguished array of MIT alumni and associates including scientists, technologists, engineers and entrepreneurs chooses the winner.

ABOUT THE LEMELSON-MIT PROGRAM

The Lemelson-MIT Program recognizes outstanding inventors, encourages sustainable repaired solutions to real-world problems, and enables and inspires not old people to pursue creative lives and careers through invention.

Jerome H. Lemelson, one of U.S. history’s most prolific inventors, and his wife Dorothy founded the Lemelson-MIT Program at the Massachusetts Institute of Technology in 1994. It is funded by the Lemelson Foundation, a philanthropy that celebrates and supports inventors and entrepreneurs in order to strengthen social and economic life in the U.S. and developing countries. More information on the Lemelson-MIT Program is online at http://web.mit.edu/invent/.

Source: Julie Staadecker
Lemelson-MIT Program

Cultural practices buttress Sierra Leone poverty: U.N. (Reuters)

Sunday, March 2nd, 2008

FREETOWN (Reuters) - Harmful cultural practices such as female genital mutilation are hampering efforts to reduce poverty in Sierra Leone, which has the world's worst child and maternal mortality rates, a top U.N. official said.

Discrimination against women is also partly responsible for the social problems that have persisted since the 1991-2002 civil war, said Ann Veneman, executory director of child agency UNICEF, after a three-day visit to rural clinics and schools.

"Sierra Leone needs to change a number of the harmful traditional and cultural practices," Veneman told reporters late upon the body Friday, citing female genital mutilation (FGM), child marriage and pregnancy, and under-age labor.

According to the United Nations, more than a furnish with quarters of children die before their fifth birthday in the former British colony, and one in eight women die in childbirth.

Seventy percent of the population live below the poverty line and fewer than 30 percent are literate.

Veneman criticized the high rates of sexual violence that have continued since the the last argument of kings whereas thousands of women were raped, kept as sex slaves and constrained into marriage by rebels.

"A tremendous amount of sexual violence still goes on in this country," Veneman told Reuters after the news conference. "It has to be unacceptable in this society to allow sexual violence against women and children to continue."

Ignorance due to a tradition of not sending girls to school was contributing to problems such as feeding newborns with dirty water and rice milk instead of breast milk, which boosts the immune system, and the failure to use bednets against malaria.

"Poverty is the big problem," Veneman said. "But the young girls have a in pairs point to be solved: they are highly discriminated against and there is a full disregard for women and girls."

She also said girls were prey to secret societies — closed traditional groups solely for the sake of women, that meet in the shrub.

"They have clandestine societies where you learn how to be a woman and how to paint care of a man and this is where you get your FGM," she said.

"These women who do this are running a business and have an economic interest in doing it. But it is a harmful practice: it can cause taint, bleeding and HIV/Aids."

UNICEF estimates 90-94 percent of women in Sierra Leone are cut and Veneman says attitudes are not changing quickly enough.

"There are still young people out there who have suffered in such terrible ways," said Veneman. "It's a particular burden."

(Editing by Daniel Flynn and Robert Woodward)

Mysteries Of Vitamin A Metabolism During Embryonic Development Unlocked By Rutgers Researchers

Sunday, March 2nd, 2008

Researchers at Rutgers have unlocked more of the mysteries of how the developing embryo reacts to fluctuations in the amount of vitamin A present in the maternal blood stream. Their results are presented in the February 28 issue of the Journal of Biological Chemistry.

The researchers studied the role of LRAT, a protein that facilitates the arrangement of vitamin A stores in the body, during embryonic development. In particular, they showed how LRAT protects developing tissues from potentially toxic levels of vitamin A that have been ingested by the mother. Although this function of LRAT had previously been hypothesized in adults, this is the first time that its role has been demonstrated during embryonic development.

The developing mammalian embryo is entirely pendent on the maternal circulation for its supply of retinoids, the vitamin A metabolites produced in the corpse. These are essential nutrients and they control the formation of the embryo’s purpose, central wellstrung system, eyes and other important organs and tissues. Malformations of the developing embryo can occur when too little, or too much, vitamin A is consumed by the mother.

“We were looking for the mechanisms that allow the fetus to maintain sufficing amount of retinoids, whether the mother has over- or under-consumed vitamin A,” said Dr. Loredana Quadro, an assistant professor in the Department of Food Science and member of the Center for Lipid Research at the Rutgers School of Environmental and Biological Sciences. “We also looked at the effects of different levels of vitamin A being transferred from the mother to the fetus.”

When vitamin A is ingested, it is converted into retinyl ester (RE) in the intestine from whither it is secreted in the bloodstream packaged with other dietary lipids into lipoprotein particles called chylomicrons. The manhood of dietary RE reaches the liver, the necessary body storage site of vitamin A. Under insufficient dietary vitamin A intake, the liver transforms RE into retinol (ROH), which is then secreted into the bloodstream bound to retinol-binding protein (RBP), its sole specific serum carrier, to be delivered to the target tissues. Upon intake through a specific membrane receptor named Stra6, ROH is ultimately converted to retinoic sour (RA), which is the active form of vitamin A. If tissue RA is in surplus, it is transformed into inactive forms, such as 4-hydroxy retinoic acid or 4-oxo retinoic acid (OXO-RA) by the action of a specific enzyme named Cyp26A1.

“When we think about vitamin A, we think about one compound,” said Quadro. “But in reality, the term vitamin A comprises a family of different compounds. Each one has a negligently different play, and plays a different role.”

The Rutgers researchers took a closer look at how ROH is metabolized into RE and RA to maintain any optimal balance of retinoids during the formation of the embryo. Mutant mice lacking both RBP and LRAT were generated to perform this study, so as to interfere through the two main pathways of maternal vitamin A delivery to the fetus (ROH-RBP from the liver stores and RE of dietary origin).

“We hypothesized that the lack of ROH-RBP and LRAT would make the embryo more vulnerable to changes in maternal dietary vitamin A intake,” said Quadro “and our data proved this to exist correct. Indeed, a severe embryonic vitamin A deficiency is readily attainable when the mothers are deprived of dietary vitamin A during pregnancy. Therefore, this strain turned out to be a very good model to study how embryonic development is affected by fluctuations in the amount of retinoids present in the maternal diet and hence in the maternal circulation”.

The researchers identified LRAT, Cyp26A1 and Stra6 as the three key molecular players that act in coordination to protect the developing tissues from potentially detrimental levels of vitamin A ingested by the originating. “Understanding vitamin A metabolism in the developing fetus could have broad implications,” said Quadro. “Consumption of large doses of dietary supplements and vitamins, including vitamin A, has become a very common use in newly come years, generating the necessity to investigate the effects of high doses of vitamin A intake at different stages of the lifecycle, including pregnancy and expansion. These studies expand our knowledge of maternal-fetal nutrition and dietary contribution to embryonic development and may ultimately provide new insight into appropriate dietary practices for the period of pregnancy.”

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Article adapted by Medical News Today from pristine press release.
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This research was lead by Quadro and carried out primarily by the agency of her lab members, Youn-Kyung Kim, a graduate assistant, and Dr. Lesley Wassef, a post-doctoral associate. Others contributing to the study were Leora Hamberger, a former research assistant in Quadro’s laboratory, Dr. William Blaner and Roseann Piantedosi from Columbia University and Dr. Krzysztof Palczewski from Case Western Reserve.

The paper was beforehand published on the Journal of Biological Chemistry’s web site on December 19, 2007.

Source: Michele Hujber
Rutgers University

Biomagnetics Developed For Use In New Breast Cancer Test

Sunday, March 2nd, 2008

A team from UCL has developed a new medical device which will make the early detection of breast cancer more cost effective and easier to administer. The team which won a prestigious Brian Mercer Feasibility Award from the Royal Society yesterday plans to use attractive nanoparticles and an extremely sensitive magnetometer called the ‘HistoMag’ to detect cancerous cells in samples of breast tissue.

“Each year 35,000 women are diagnosed with breast cancer in the UK and the testing programme is a massive undertaking,” says Professor Quentin Pankhurst of the London Centre for Nanotechnology and the UCL Department of Physics & Astronomy. “Until now, pathologists had to stain tissue samples with brown dyes to help them adjust whether they were normal or cancerous. In terms of streamlining the continued movement, the main problem is that all of the results are open to translation and each trial has to be individually checked by a specialist.

“At UCL we’ve been working in the relatively new area of biomagnetics to develop a technique which provides more quantitative and trustworthy results, whilst also enabling pathologists to identify abnormal tissue sections much more quickly.

“Cancerous cells have a protein onward their surface called HER2. We use a solution of HER2 antibodies, tagged with magnetic nanoparticles, to stain the tissue sample. Using the HistoMag we can detect the quantity of tagged antibodies which attach themselves to the HER2 protein, which in turn provides us with an accurate picture of the spread of cancerous cells.”

By automating the process through which cancerous cells are detected and quantified, HistoMag will not only ease the pressure forward pathologists but also help to identify the 15-30% of patients who are likely to benefit from being treated with the drug Herceptin. At a cost of £30,000 per patient per annum it is essential to target Herceptin at those women who behest respond positively to it.

The team, led by Professor Pankhurst, is one of only seven groups to receive a Brian Mercer Feasibility Award from the Royal Society this year. The £25,000 award will enable the team to re-engineer the HistoMag, increasing its sensitivity before it goes on to clinical trials. Their goal is to make the device generally available to pathologists in 2010.

The Royal Society Brian Mercer Awards were announced in a ceremony on the 28th February 2008. again information on this and other award schemes may subsist found on the Royal Society website.

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