Articles tagged with Cancer Genetics
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Researchers found that patients with a family history of pancreatic cancer are more likely to be diagnosed at an earlier age and have a smoking history. The study suggests that strong counseling against smoking is necessary for these patients, as well as smoking cessation programs.
A recent study found that demethylation agents not only restart cancer-suppressing genes but also knock methyl groups off other genes, turning hundreds more off. The research raises concerns about the impact of these agents on gene expression and their potential to exacerbate cancer development.
Researchers create strategy to trick ATM gene into overlooking premature termination codons, restoring full-length protein production and alleviating symptoms. The treatment uses aminoglycosides to make PTCs invisible to the cell's machinery, showing promise for halting disease progression and cancer risk in A-T patients.
A team of Hopkins researchers is using new genome searching technologies to identify genetic factors contributing to autism. They will analyze data from 465 families and 979 individuals with autism, focusing on rare genetic mutations and extra or missing gene copies.
Researchers have discovered a new mechanism for the formation of active cancer genes in T-cell acute lymphatic leukemia (T-ALL), leading to an uncontrolled growth of immature white blood cells. The study suggests using Glivec, a kinase inhibitor that targets ABL1, as a potential treatment for T-ALL patients.
A genetic predictive test identifies brain cancer patients who benefit from temozolomide, a targeted treatment. The study found a 46% survival rate for those with methylated MGMT promoter status.
A Phase II study has shown that the drug imatinib is active against a rare type of cancer called DFSP, achieving complete control in eight out of ten patients. The research team believes molecular analysis can predict patient response to treatment based on genetic profiles.
Researchers at Ohio State University have identified five genes that can distinguish between papillary thyroid carcinoma (PTC) and follicular thyroid carcinoma (FTC), two types of thyroid cancer with different behaviors and treatments. The study's findings may lead to a valuable diagnostic tool, improving patient outcomes.
Researchers at Temple University's Sbarro Institute developed a new blood test that uses CDK9/CYCLIN T1 expression to accurately diagnose lymphoma cancer types and stages. The study, published in the Journal of Pathology, found that analyzing these molecules in a blood sample can pinpoint the presence of lymphoma with high accuracy.
Researchers have found that the threespine stickleback fish has a genetic sex-determination system similar to other vertebrates, with females having XX chromosomes and males having XY. The study provides evidence for the early formation of sex chromosomes in this species, offering insights into the evolution of sex chromosomes.
African-American women are less likely to undergo immediate or delayed breast reconstruction after mastectomy compared to Caucasian, Hispanic, Asian, and Middle Eastern women. Physicians' referral patterns and patient acceptance also contribute to these racial discrepancies.
Researchers have identified strong evidence for a prostate cancer gene on chromosome 17, which is also known to harbor the breast cancer gene BRCA1. A separate study found that a variant of the MIC-1 gene, involved in inflammation, is associated with a decreased risk for prostate cancer.
Researchers found that IKK beta deletion in epithelial cells decreases cancer incidence and tumor growth in mice by up to 80%. In myeloid cells, IKK beta deletion also reduces pro-inflammatory molecule expression, leading to smaller tumors. This study establishes the role of IKK beta in inflammation-associated tumor promotion.
Researchers successfully cloned mice from malignant cancer cells using nuclear transfer. The study reveals that the epigenetic elements of cancer can be reversed, whereas genetic mutations are not.
Researchers found genes in stromal cells were overactive in early and late-stage breast cancer specimens. Targeting these components with cancer drugs might improve treatment effectiveness. The study identified two potential therapeutic targets: CXCL12 and CXCL14.
Researchers identified 671 genes with altered expression in prostate cancer tissue, revealing a high degree of similarity between benign adjacent tissue and cancerous tissue. The study found that genetic alterations occur throughout the gland, even in seemingly benign areas, providing new insights into prostate cancer progression.
A study found that HPV DNA is present in tumors of HNSCC patients, suggesting a role for the virus in early cancer development. The findings support the idea that HNSCCs can be subdivided into two genetically distinct categories, one driven by environmental factors and the other by HPV infection.
Knudson was awarded the basic sciences prize for his role in establishing the theory of tumor suppressor genes, which opened a new horizon in modern cancer genetics. His work holds implications for both treatment and prevention, and has led to advances in understanding human cancer.
Researchers developed a reliable animal model to test new drugs for retinoblastoma, a deadly childhood cancer. The model has already identified a promising new treatment being studied in clinical trials.
Researchers have developed a gene therapy that protects bone marrow cells from chemotherapy's debilitating effects. The study found up to 41% transfer of the protective gene to blood stem cells in patients with advanced cancer, offering new hope for improved treatments.
A study of 494 cancer patients found that specific genetic variants are associated with increased fatigue and distress, suggesting a possible link between genetics and quality of life in cancer patients. The research aims to develop personalized treatments tailored to an individual's genetic profile to improve their quality of life.
Dr. Bernard Levin, a colorectal cancer expert, is honored by ASCO for his significant contributions to preventing and managing cancer. He will deliver an acceptance lecture on June 6, highlighting his leadership in multidisciplinary programs in research, service, and education.
Researchers have identified a critical regulatory region for the development of the enteric nervous system, which plays a vital role in gastrointestinal functions. Genetic mutations in this region may lead to incomplete development of the enteric nervous system, often causing Hirschsprung disease.
A study found that African-Americans are 1.67 times more likely to die within five years and 1.52 times more likely to die within ten years after surgical treatment for CRC compared to Caucasians. Racial differences were most pronounced in patients with stage II disease.
Researchers analyzed DNA samples from 414 dogs representing 85 breeds to discover previously unappreciated relationships between existing breeds. They found four genetic clusters, including a cluster containing ancient breeds with wolf-like ancestry.
Researchers use zebrafish to study human heart valve formation and cancer risk, identifying novel actin molecules and ribosomal protein genes that predispose fish to malignant tumors. The findings suggest a causal relationship between early heart function and its final structure.
Researchers report first clinical experience of preimplantation HLA matching, demonstrating feasibility for stem cell transplantation in siblings with bone marrow failure. The study involved nine couples with children affected by blood disorders and resulted in five healthy children who were HLA-matched to their affected siblings.
Researchers identified a 23-gene signature that can predict disease recurrence in Dukes' B colon cancer patients with high accuracy. The study's findings have significant implications for personalized therapy decisions and could lead to improved patient outcomes.
A recent study has found a dramatic increase in lung cancer incidence in women, with many cases occurring in non-smokers who stopped smoking years ago. The study also reveals that women's response to targeted therapies is more favorable than men, raising questions about the differences between male and female lung cancer.
The grant will fund studies on how the enzyme, DNA polymerase, accurately copies genetic information, revealing its unique catalytic selectivity and minimizing errors, which could inform cancer research.
Scientists at Fox Chase Cancer Center successfully extracted high-quality RNA from archived tissue samples using the Paradise Reagent System. This innovation allows researchers to identify genetic changes in cancer that span years, enabling personalized therapy.
Researchers found 53 smoking-induced genetic alterations in mice exposed to tobacco smoke, with CYP1B1 enzyme overexpression linked to estradiol activation. This finding may help understand why female smokers are more susceptible to lung cancer than male smokers.
Webster Cavenee receives $250,000 grant from National Foundation For Cancer Research to study cancer tumors. His research focuses on defining genetic lesions in human cancer and developing therapeutic approaches.
The AACR International Scholars in Breast Cancer Research program aims to improve cancer research and clinical care worldwide. Principal Investigators will mentor talented scientists from under-resourced countries, enhancing their skills and knowledge for successful breast cancer research.
A new diagnostic tool, BCPC, uses microarray technology to analyze tumor genetic signatures and provide personalized treatment recommendations for breast cancer patients. The tool aims to improve patient outcomes by avoiding over-treatment and reducing costs of treatment.
A new tumor classification system combines molecular biology and classic pathology to provide a comprehensive and consistent way of typing tumors. The system uses both the type of cells that form a tumor and its molecular characteristics to determine its behavior, offering improved accuracy and insight into treatment options.
Researchers have developed a gene expression profiling method that predicts clinical outcome in prostate cancer patients. The study's findings suggest that this approach can improve our ability to stratify patient populations and optimize disease treatment.
Researchers found that switched-off SFRP genes allow the WNT pathway to stay active, leading to colon cell growth and tumor formation. The study suggests that reactivating SFRPs may prevent colon cancer by stopping this chain reaction.
Novel genetic profiling can identify residual tumors and precancerous lesions, allowing for targeted treatment. Early clinical trials show promise for gene-mediated strategies to replace defective sequences and block signal transduction.
Researchers at Duke University Medical Center have discovered a gene link between juvenile polyposis and high blood pressure syndrome. The study suggests that patients with the intestinal disorder should undergo genetic screening for vascular defects, as they are at risk of experiencing severe nosebleeds or strokes.
Researchers found a significant increase in cancer cases among teenagers and young adults, with certain cancers dominating at different ages. The study suggests that environmental risk factors and genetic susceptibility may play a role in the increasing incidence of adolescent and young adult cancer.
A recent study, PROSE, found that double mastectomies significantly reduce the risk of breast cancer in women with BRCA1 and BRCA2 gene mutations by 95%. The study followed 483 at-risk women for over six years, showing that prophylactic mastectomies can be an effective preventive measure.
Researchers have discovered a new hereditary cancer mutation associated with an increased risk of colon, endometrial and ovarian cancers. The mutation was found in descendants of a German immigrant who arrived in the US in 1727.
A new theory by Steven Frank proposes that cancer progression speeds up with age, leading to increased incidence in older adults. As people age, fewer stages remain before cancer develops, resulting in higher cancer rates.
A study published in Nature Biotechnology found that the Sindbis virus is effective at killing tumors in mice, with varying time and injection schedules required. The virus targets tumor cells by binding to a specific receptor, making it a potential tracking device for cancer.
A study published in Science reveals that the overwhelming source of human genetic variation is between individuals, not ethnic groups. The research also highlights the importance of multi-disciplinary collaboration in advancing medical knowledge.
Researchers have discovered that Heat shock protein (Hsp) 70.1 and 70.3 can be used to increase cancer cells' vulnerability to radiation treatments, offering a new treatment window for cancer patients. The proteins were found to interact with telomerase, an enzyme that helps maintain the telomeres at the ends of chromosomes.
The International HapMap Project aims to map the locations of representative tag SNPs in DNA samples from diverse populations. The project's results will increase the power and reduce the cost of future genetic association studies, significantly speeding up the discovery of genes involved in common diseases.
Researchers have developed a mouse model that mimics human pancreatic cancer, enabling the discovery of biomarkers for early detection and potential therapeutic targets. The model replicates the disease's progression and is poised to facilitate rapid testing of novel treatments.
Research suggests that air travel increases the risk of blood clots, particularly in individuals with genetic predispositions and those taking oral contraceptives. Long-haul flights lasting eight hours or longer may double the risk of isolated calf muscle venous thrombosis.
A study found that patients with high levels of low molecular weight cyclin E have aggressive, invasive breast cancer, and the protein may be a better predictor of patient outcome than current markers. This altered form of cyclin E can induce genetic instability, making tumors unresponsive to treatment.
Researchers at Fox Chase Cancer Center discovered a novel DNA-repair gene mutation that causes resistance to cancer drugs, particularly in colorectal cancer. The defective MED1 enzyme interferes with chemotherapy's effectiveness, making cancers resistant to widely used treatments.
Researchers at St. Jude Children's Research Hospital have developed a new gene profiling technique that could simplify diagnostic tests for acute lymphoblastic leukemia (ALL), a childhood cancer with an 80% success rate due to risk-adapted therapy.
Scientists at Stanford University have created a 'supersized' DNA molecule, xDNA, consisting of larger base pairs that can increase stability and fluorescence. This new genetic system has the potential to revolutionize medical biopsies and potentially lead to the discovery of new life forms.
Dr. Yuan Chang discovered human herpesvirus 8 (KSHV) in 1994 and has since studied its biology to understand how it causes cancer. Her work has transformed understanding of the most common malignancy in people infected with HIV.
A new model of cancer development suggests that Id1 activation may be crucial for tumor growth, contradicting previous research. The study, which used mice exposed to carcinogens, found that tumors developed faster in mice without the Id1 gene.
Researchers discovered a genetic link between prostate cancer and a specific gene variant, CYPIBI. The study found that tiny variations in the gene may increase or decrease its cancer-causing effects, leading to a higher risk of developing prostate cancer.
A new study identifies a specific DNA stretch on chromosome 9 that houses a susceptibility gene linked to increased colon cancer risk. Researchers analyzed blood samples from 53 families affected by colon cancer or pre-cancerous polyps and found a common genetic link.
Dr. Hong's work has accelerated the pace of growth in cancer prevention research, opening doors to less toxic and more effective chemopreventive agents and regimens. His research has demonstrated the effectiveness of biochemoprevention in reducing both primary and recurrent cancers.
The study found that methylation levels in a specific gene can predict the seriousness of breast cancer. High levels of promoter methylation correlate with an altered structure of the gene, resulting in a tightly closed DNA configuration that prevents gene activation.