Popular Articles

Fanconi Anemia: Genetically Corrected Blood Cells Obtained From Patients' Skin Cells
Collaboration research carried out by the teams of Jordi Surrallés, Universitat Autònoma de Barcelona (UAB); Juan Carlos IzpisÃôa-Belmonte and Angel Raya, Centre for Regenerative Medicine of Barcelona (CMRB); and Juan Antonio Bueren, Centre for Energetic, Environmental and Technological Research (CIEMAT), has resulted in the generation of blood cells from skin cells of patients with a genetic disease known as Fanconi anemia. The process is based on gene therapy and cell reprogramming techniques in which cells similar to embryonic stem cells known as induced pluripotent stem (iPS) cells can be generated. The research article was published in this week"s digital version of Nature.
òåëåôîí nokia c203
Oakland, Calif., Conference Targets Black Women For HIV/AIDS Awareness, Prevention
The Oakland, Calif., chapter of the National Coalition of 100 Black Women on Saturday held a daylong conference, "Sistahs Getting Real About HIV/AIDS," that addressed HIV/AIDS among black women, the San Francisco Chronicle reports. The conference "focused on two issues that might seem contradictory: first, to convince women that they must take special precautions to protect themselves, and second, to let them know that an HIV diagnosis is not a death sentence," according to the Chronicle. Keynote speaker of the conference Tony Wafford, director of health and wellness for the National Action Network, said black women need to be more vocal with their partners about practicing safe sex and getting tested for HIV. Organizers noted that black women also "must address the stigma associated with HIV before they can talk openly about the risk of infection with their partners," the article states (Allday, 7/25).
ìîíèòîðû â ëóãàíñêå
News of the day
Glimpsing The Birth Of Our Earliest Reproductive Cells
It has long been a mystery how the developing embryo designates those rare, precious cells destined to produce sperm and eggs -- enabling us to have offspring - since these primordial germ cells" existence is fleeting and hard to spot with the tools of biology. Now, using mouse embryonic stem cells, researchers in the Stem Cell Program at Children"s Hospital Boston have managed to recapitulate the creation of primordial germ cells (PGCs) in the lab, capturing the stem cells" gene activity as they differentiated to form PGCs. The findings, published in the July 5 issue of Nature, also offer a unique window on cancer.
Oncology

UNMC Scientists ID Molecule Superfamily That Causes Melanoma Spread

A University of Nebraska Medical Center research team has determined that a superfamily of molecules hold the secret to the progression and spread of melanoma -- the deadliest form of skin cancer. The study results were published in today"s issue of the British Journal of Cancer. UNMC researcher Seema Singh, Ph.D., a research associate in the laboratory of Rakesh Singh, Ph.D., has investigated the roles of a superfamily of small molecules called "chemokines" and their receptor "partner molecules" in melanoma development. Dr. Rakesh Singh"s research team "turned up" the normal activity of two particular receptor molecules called CXCR1 and CXCR2 inside human melanoma cell lines and studied the effect on cancer progression and tumor growth using a mouse model. Their results suggested that CXCR1 and CXCR2 play key roles in the progression and spread of melanoma. The scientists found that the molecules helped tumor cells to grow. And when they "turned up" the activity of CXCR1 and CXCR2 in healthy cells it triggered tumor formation. Chemokines together with their receptor partner molecules control the movement of many types of cells in the body. Scientists already knew that some molecules from this superfamily regulated the movement of certain types of healthy cells in the body"s lymphoid system and thought that chemokines also might control the migration of tumor cells in the body. Several studies have implicated CXCR1 and CXCR2 as important players in tumor progression. Dr. Rakesh Singh, UNMC professor of pathology/microbiology and lead author, said the findings may lead to significant diagnostic and therapeutic advances. "These results suggest that a superfamily of molecules controls whether a melanoma advances and spreads to other parts of the body -- when it becomes difficult to treat," Dr. Rakesh Singh said. "There is a possibility these molecules could be used in future therapy for melanoma -- something that doesn"t exist at the moment." Based on earlier research that he published in April"s Clinical Cancer Research journal, Dr. Rakesh Singh knows these same receptors can play an important role in melanoma growth. "We have evidence that they are good targets to inhibit growth," he said. "In cancer cells, these molecules may be over expressed and their function compromised." "This important research gives us a start to understanding how malignant melanoma progresses and spreads," said Dr. Lesley Walker, director of cancer information at Cancer Research UK. Melanoma accounts for roughly 4 percent of all skin cancers, but is responsible for more than 74 percent of skin cancer deaths. Malignant melanoma is the most aggressive form of skin cancer with a very poor prognosis. The tumor originates in melanocytes, the cells which produce the pigment melanin that colours our skin, hair and eyes. If detected and treated early, it is easy to treat. But if it is ignored the cancer can advance and spread to other parts of the body, where it becomes hard to treat and can be fatal. University of Nebraska Medical Center Public Relations Department


Add your comment:
Name:
Site address: http://
Your message:
Enter today\\\\'s date, 2 digits
(spam protection):