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Latest Journal Index
- 11 March 2010 Accomplishments in 2007 in the adjuvant treatment of rectal cancer.
- 11 March 2010 Clinical utility of the assessment of fecal calprotectin in Leśniowski-Crohn's disease.
- 05 March 2010 Initial testing (stage 1) of lapatinib by the pediatric preclinical testing program.
- 13 February 2010 Advances in radiotherapy in operable rectal cancer.
- 13 February 2010 Total mesorectal excision for rectal cancer in an unselected population: quality assessment in a low volume center.
- 12 February 2010 Lymph node counts and survival rates after resection for colon and rectal cancer.
- 12 February 2010 Time to Redefine the Role of Routine Combined-Modality Therapy for Invasive Stage-II/III Rectal Cancer?
- 12 February 2010 Total pelvic exenteration for primary and recurrent malignancies.
- 12 February 2010 Clinical significance of Neutrophil gelatinase-associated lipocalin(NGAL) expression in primary rectal cancer.
- 12 February 2010 The effect of provider case volume on cancer mortality: systematic review and meta-analysis.
- 12 February 2010 Oral contraceptives and colorectal cancer risk: a systematic review and meta-analysis.
- 12 February 2010 Local excision of early rectal cancer: is transanal endoscopic microsurgery an alternative to radical surgery?
- 12 February 2010 The plasticity of the defecation reflex pathway in the enteric nervous system of guinea pigs.
- 11 February 2010 Neoadjuvant concurrent chemoradiotherapy in treating locally advanced rectal cancer.
- 11 February 2010 Reverse transcription-quantitative polymerase chain reaction: description of a RIN-based algorithm for accurate data normalization.
- 11 February 2010 A kernel-based integration of genome-wide data for clinical decision support.
- 11 February 2010 Crohn's disease and early exposure to domestic refrigeration.
- 11 February 2010 Tryptophan degradation in irritable bowel syndrome: evidence of indoleamine 2,3-dioxygenase activation in a male cohort.
- 11 February 2010 Treatments for irritable bowel syndrome: patients' attitudes and acceptability.
- 10 February 2010 Defining preoperative treatment strategies in t3 rectal cancer.
- 10 February 2010 Adjuvant treatment of colorectal cancer.
- 10 February 2010 Needle track seeding: a real hazard after percutaneous radiofrequency ablation for colorectal liver metastasis.
- 10 February 2010 Microvessel density as new prognostic marker after radiotherapy in rectal cancer.
- 10 February 2010 Prognostic factors for 5-year survival after local excision of rectal cancer.
- 10 February 2010 Effect of the plane of surgery achieved on local recurrence in patients with operable rectal cancer: a prospective study using data from the MRC CR07 and NCIC-CTG CO16 randomised clinical trial.
- 10 February 2010 Neural and psychological predictors of treatment response in irritable bowel syndrome patients with a 5-HT3 receptor antagonist: a pilot study.
- 10 February 2010 Recollection of childhood abdominal pain in adults with functional gastrointestinal disorders.
- 10 February 2010 Self-reported use of pharmaceuticals among patients with irritable bowel syndrome in primary care.
- 10 February 2010 The clinical overlap between functional dyspepsia and irritable bowel syndrome based on Rome III criteria.
- 10 February 2010 Probiotic effects on intestinal fermentation patterns in patients with irritable bowel syndrome.
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Adjuvant external beam radiotherapy in the treatment of endometrial cancer (MRC ASTEC and NCIC CTG EN.5 randomised trials): pooled trial results, systematic review, and meta-analysis. Lancet. 2009 Jan 10;373(9658):137-46 Authors: , Blake P, Swart AM, Orton J, Kitchener H, Whelan T, Lukka H, Eisenhauer E, Bacon M, Tu D, Parmar MK, Amos C, Murray C, Qian W BACKGROUND: Early endometrial cancer with low-risk pathological features can be successfully treated by surgery alone. External beam radiotherapy added to surgery has been investigated in several small trials, which have mainly included women at intermediate risk of recurrence. In these trials, postoperative radiotherapy has been shown to reduce the risk of isolated local recurrence but there is no evidence that it improves recurrence-free or overall survival. We report the findings from the ASTEC and EN.5 trials, which investigated adjuvant external beam radiotherapy in women with early-stage disease and pathological features suggestive of intermediate or high risk of recurrence and death from endometrial cancer. Current treatment of metastatic endometrial cancer. Cancer Control. 2009 Jan;16(1):38-45 Authors: Temkin SM, Fleming G BACKGROUND: Endometrial cancer is the most common gynecologic malignancy. The majority of patients have disease confined to the uterus and have an excellent overall prognosis. However, subgroups of patients have advanced primary disease or recurrences following primary treatment. Gonadotropin-releasing hormone (GnRH)-I and GnRH-II induce cell growth inhibition in human endometrial cancer cells: Involvement of integrin beta3 and focal adhesion kinase. Reprod Biol Endocrinol. 2009 Aug 5;7(1):81 Authors: Park DW, Choi KC, Maccalman CD, Leung PC ABSTRACT: Endometrial carcinoma is the most common neoplasm of the female genital tract, accounting for nearly one half of all gynecologic cancers in the Western world. Although intensive research on pathological phenomena of endometrial cancer is currently going on, but exact cause and biological aspects of this disease are not well described yet. In addition to well-documented roles of gonadotropin-releasing hormone (GnRH) in hypopituitary ovarian (HPO) axis, the agonistic or antagonistic analogs (or both) of GnRH have been shown to inhibit the proliferation of a variety of human gynecologic cancers. Thus, in the present study, we further examined the possibility that GnRH induces integrin beta3 and activation of focal adhesion kinase (FAK) through mitogen-activated protein kinases (MAPKs), ERK1/2 and p38, to inhibit the growth of HEC1A endometrial cancer cell line. As a result, both GnRH-I and GnRH-II resulted in a significant increase in integrin beta3 expression and evoked the activation of FAK in a time-dependent manner in these cells. In addition, these analogs induced an activation of ERK1/2 and p38 MAPK in a time-dependent manner as downstream pathways of FAK. It appears that GnRH-II has much greater effect on the activation of FAK, ERK1/2 and p38 compared to GnRH-I in these cells. Further, we demonstrated that the growth inhibition of HEC1A cells by GnRH-I or GnRH-II is involved in the activation of integrin-FAK and ERK1/2 and p38 MAPK pathways. Taken together, these results suggest that GnRH may be involved in the inhibition of endometrial cancer cell growth via activation of integrin beta3 and FAK as a direct effect. This knowledge could contribute to a better understanding of the mechanisms implicated in the therapeutic action of GnRH and its biomedical application for the treatment against endometrial cancer. P MID: 19656390 [PubMed - as supplied by publisher] Read Full Article pubmed: endometrial cancer Potential role of UGT pharmacogenetics in cancer treatment and prevention: focus on tamoxifen. Ann N Y Acad Sci. 2009 Feb;1155:99-111 Authors: Lazarus P, Blevins-Primeau AS, Zheng Y, Sun D Tamoxifen (TAM) is a selective estrogen receptor modulator that is widely used in the prevention and treatment of estrogen receptor-positive (ER(+)) breast cancer. Its use has significantly contributed to a decline in breast cancer mortality, since breast cancer patients treated with Tamoxifen (TAM) for 5 years exhibit a 30-50% reduction in both the rate of disease recurrence after 10 years of patient follow-up and occurrence of contralateral breast cancer. However, in patients treated with TAM there is substantial interindividual variability in the development of resistance to TAM therapy, and in the incidence of Tamoxifen (TAM)-induced adverse events, including deep vein thrombosis, hot flashes, and the development of endometrial cancer. This article will focus on the UDP glucuronosyltransferases, a family of metabolizing enzymes that are responsible for the deactivation and clearance of TAM and TAM metabolites, and how interindividual differences in these enzymes may play a role in patient response to Tamoxifen (TAM). PMID: 19250197 [PubMed - indexed for MEDLINE] Read Full Article pubmed: cancer endometrial Silencing of heat shock protein 70 expression enhances radiotherapy efficacy and inhibits cell invasion in endometrial cancer cell line. Croat Med J. 2009 Apr;50(2):143-50 Authors: Du XL, Jiang T, Wen ZQ, Gao R, Cui M, Wang F AIM: To investigate the role of heat shock proteins 70 (HSP70) in radiosensitivity and invasiveness of endometrial cancer in vitro. METHODS: HSP70 expression was silenced in relatively radioresistant, well-differentiated human endometrial cancer cell line ISK, using small interference RNA method, or by HSP70 overexpression after transfecting a HSP70-expressing vector. The effect of HSP70 on ISK cell line response to irradiation was evaluated. The surviving fraction was measured using colony-formation assay. Apoptosis was detected by flow cytometry and HSP70 expression was determined by quantitative real-time polymerase chain reaction, western-blot, and/or immunocytochemistry. Cell invasiveness was measured using transwell invasion assay. RESULTS: HSP70 silencing caused a significant increase in irradiation-induced cell killing in comparison with control cells, with an enhancement factor of 1.27, and in the percentage of apoptotic cells (14.22% vs 6.74%, P = 0.021). After 4 Gy irradiation, mean +/- standard deviation survival fraction in ISK cells was reduced to 0.32 +/- 0.04 in comparison with control values but in ISK/siRNA-HSP70 cells the survival fraction was higher and amounted to 0.51 +/- 0.08 (P = 0.026). Silencing HSP70 significantly inhibited cell invasion before and after irradiation (106 +/- 19 vs 219 +/- 18 and 119 +/- 16 vs 256 +/- 31, P = 0.007). On the contrary, ectopic overexpression of HSP70 attenuated irradiation-induced apoptosis (7.15% vs 4.08%, P = 0.043) and induced more ISK/HSP70 cells invaded through the filters than mock-infected cells before and after irradiation (274 +/- 21 vs 194 +/- 16 before irradiation, and 298 +/- 24 vs 227 +/- 19 after irradiation, respectively, P = 0.032). CONCLUSION: Disruption of HSP70-induced cytoprotection during irradiation enhances therapeutic effect of irradiation, which makes HSP70 a promising target in the research of endometrial cancer. PMID: 19399947 [PubMed - indexed for MEDLINE] Read Full Article pubmed: cancer endometrial Race disparities between black and white women in the incidence, treatment, and prognosis of endometrial cancer. Cancer Control. 2009 Jan;16(1):53-6 Authors: Allard JE, Maxwell GL BACKGROUND: Uterine cancer is the most common gynecologic malignancy in the United States, with an estimated 40,100 new cases and 7,470 deaths occurring in 2008. Although the incidence of endometrial cancer is lower among black women compared with white women, the proportion of cancer-related deaths among blacks is higher and has continued to rise over the past two decades. The role of comprehensive surgical staging in patients with endometrial cancer. Cancer Control. 2009 Jan;16(1):23-9 ; Authors: Frederick PJ, Straughn JM BACKGROUND: The cornerstone of the management of patients with endometrial cancer is hysterectomy. Since 1988, the role of lymphadenectomy for patients with endometrial cancer has been debated. Patients who undergo pelvic and para-aortic lymphadenectomy are more likely to be accurately staged and are less likely to receive adjuvant radiation therapy. The use of minimally invasive surgery for endometrial cancer. Cancer Control. 2009 Jan;16(1):30-7 Authors: Humphrey MM, Apte SM BACKGROUND: Endometrial cancer is the most common gynecologic malignancy in the United States. Surgical staging is an integral component in the treatment of this disease. Minimally invasive surgical techniques have been utilized with increasing frequency in its management. |
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