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Small cell lung cancer

KEGG ID: hsa05222

中文名称

小细胞肺癌

通路描述

肺癌是工业化国家男性和女性癌症死亡的首要原因。小细胞肺癌(SCLC)是一种高度侵袭性肿瘤,约占所有肺癌病例的 25%。SCLC 中改变的分子机制包括诱导癌基因(MYC)的表达和肿瘤抑制基因(如 p53、PTEN、RB 和 FHIT)的丢失。SCLC 中 MYC 蛋白的过表达主要是由基因扩增引起的。这种过表达导致更快的增殖和终末分化丧失。p53 或 PTEN 的突变或缺失可导致更快的增殖和减少的凋亡。视网膜母细胞瘤基因 RB1 编码一种核磷酸蛋白,有助于调节细胞周期进展。脆弱组氨酸三叠体基因 FHIT 编码酶 diadenosine triphosphate 水解酶,被认为在细胞凋亡和细胞周期控制中起间接作用。
英文描述
Lung cancer is a leading cause of cancer death among men and women in industrialized countries. Small cell lung carcinoma (SCLC) is a highly aggressive neoplasm, which accounts for approximately 25% of all lung cancer cases. Molecular mechanisms altered in SCLC include induced expression of oncogene, MYC, and loss of tumorsuppressor genes, such as p53, PTEN, RB, and FHIT. The overexpression of MYC proteins in SCLC is largely a result of gene amplification. Such overexpression leads to more rapid proliferation and loss of terminal differentiation. Mutation or deletion of p53 or PTEN can lead to more rapid proliferation and reduced apoptosis. The retinoblastoma gene RB1 encodes a nuclear phosphoprotein that helps to regulate cell-cycle progression. The fragile histidine triad gene FHIT encodes the enzyme diadenosine triphosphate hydrolase, which is thought to have an indirect role in proapoptosis and cell-cycle control.

所含基因

93 个基因