Identification of genes associated with gall bladder cell carcinogenesis: Implications in targeted therapy of gall bladder cancer

被引:0
|
作者
Ghosh, Ishita [1 ]
Dey Ghosh, Ruma [1 ]
Mukhopadhyay, Soma [1 ,2 ]
机构
[1] Netaji Subhas Chandra Bose Canc Res Inst, Dept Mol Biol, Kolkata 700094, India
[2] Netaji Subhas Chandra Bose Canc Res Inst, Dept Mol Biol, 3081 Nayabad, Kolkata 700094, India
关键词
Gall bladder cancer; Gene biomarker; Targeted therapy; siRNA mediated therapy; Prognosis; Advanced therapy of gall bladder cancer; MIGRATION INHIBITORY FACTOR; LYMPHOCYTIC-LEUKEMIA CELLS; BILIARY-TRACT CANCERS; GALLBLADDER CARCINOMA; K-RAS; EXPRESSION; ACTIVATION; GROWTH; CD44; P53;
D O I
10.4251/wjgo.v15.i12.2053
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gall bladder cancer (GBC) is becoming a very devastating form of hepatobiliary cancer in India. Every year new cases of GBC are quite high in India. Despite recent advanced multimodality treatment options, the survival of GBC patients is very low. If the disease is diagnosed at the advanced stage (with local nodal metastasis or distant metastasis) or surgical resection is inoperable, the prognosis of those patients is very poor. So, perspectives of targeted therapy are being taken. Targeted therapy includes hormone therapy, proteasome inhibitors, signal transduction and apoptosis inhibitors, angiogenesis inhibitors, and immunotherapeutic agents. One such signal transduction inhibitor is the specific short interfering RNA (siRNA) or short hairpin RNA (shRNA). For developing siRNA-mediated therapy shRNA, although several preclinical studies to evaluate the efficacy of these key molecules have been performed using gall bladder cells, many more clinical trials are required. To date, many such genes have been identified. This review will discuss the recently identified genes associated with GBC and those that have implications in its treatment by siRNA or shRNA.
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页数:12
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