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肺肿瘤细胞系中凋亡调控基因的表达:与p53表达的关系及与获得性耐药的相关性

Expression of apoptosis-regulatory genes in lung tumour cell lines: relationship to p53 expression and relevance to acquired drug resistance.

作者信息

Reeve J G, Xiong J, Morgan J, Bleehen N M

机构信息

Medical Research Council Clinical Oncology and Radiotherapeutics Unit, Medical Research Council Centre, Cambridge, UK.

出版信息

Br J Cancer. 1996 May;73(10):1193-200. doi: 10.1038/bjc.1996.230.

DOI:10.1038/bjc.1996.230
PMID:8630278
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2074502/
Abstract

As a first step towards elucidating the potential role(s) of bcl-2 and bcl-2-related genes in lung tumorigenesis and therapeutic responsiveness, the expression of these genes has been examined in a panel of lung cancer cell lines derived from untreated and treated patients, and in cell lines selected in vitro for multidrug resistance. Bcl-2 was hyperexpressed in 15 of 16 small-cell lung cancer (SCLC) cell lines and two of five non-small-cell lung cancer (NSCLC) lines compared with normal lung and brain, and hyperexpression was not chemotherapy related. Bcl-x was hyperexpressed in the majority of SCLC and NSCLC cell lines as compared with normal tissues, and all lung tumour lines preferentially expressed bcl-x1-mRNA, the splice variant form that inhibits apoptosis. Bax gene transcripts were hyperexpressed in most SCLC and NSCLC cell lines examined compared with normal adult tissues. Mutant p53 gene expression was detected in the majority of the cell lines and no relationship between p53 gene expression and the expression of either bcl-2, bcl-x or bax was observed. No changes in bcl-2, bcl-x and bax gene expression were observed in multidrug-resistant cell lines compared with their drug-sensitive counterparts.

摘要

作为阐明bcl-2及bcl-2相关基因在肺癌发生和治疗反应中潜在作用的第一步,已对一组来源于未经治疗和经治疗患者的肺癌细胞系,以及体外筛选出的多药耐药细胞系中这些基因的表达进行了检测。与正常肺组织和脑组织相比,16个小细胞肺癌(SCLC)细胞系中的15个以及5个非小细胞肺癌(NSCLC)细胞系中的2个bcl-2呈高表达,且高表达与化疗无关。与正常组织相比,大多数SCLC和NSCLC细胞系中bcl-x呈高表达,并且所有肺肿瘤细胞系均优先表达bcl-x1-mRNA,即抑制细胞凋亡的剪接变异体形式。与正常成人组织相比,在所检测的大多数SCLC和NSCLC细胞系中Bax基因转录本呈高表达。在大多数细胞系中检测到突变型p53基因表达,未观察到p53基因表达与bcl-2、bcl-x或bax表达之间存在关联。与药敏细胞系相比,多药耐药细胞系中bcl-2、bcl-x和bax基因表达未发生变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/07949ab76419/brjcancer00038-0041-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/58c4ee12c1d1/brjcancer00038-0039-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/2039a3dcf8f3/brjcancer00038-0040-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/a4d61db27390/brjcancer00038-0041-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/548a9b192f35/brjcancer00038-0041-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/07949ab76419/brjcancer00038-0041-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/58c4ee12c1d1/brjcancer00038-0039-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/2039a3dcf8f3/brjcancer00038-0040-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/a4d61db27390/brjcancer00038-0041-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/548a9b192f35/brjcancer00038-0041-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa4c/2074502/07949ab76419/brjcancer00038-0041-c.jpg

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本文引用的文献

1
Apoptosis of lung cancer cells caused by some anti-cancer agents (MMC, CPT-11, ADM) is inhibited by bcl-2.
Biochem Biophys Res Commun. 1993 Apr 15;192(1):30-6. doi: 10.1006/bbrc.1993.1377.
2
Constitutive expression of human Bcl-2 modulates nitrogen mustard and camptothecin induced apoptosis.人Bcl-2的组成型表达可调节氮芥和喜树碱诱导的细胞凋亡。
Cancer Res. 1993 Apr 15;53(8):1853-61.
3
Expression of BCL-2 protein enhances the survival of mouse fibrosarcoid cells in tumor necrosis factor-mediated cytotoxicity.BCL-2蛋白的表达增强了小鼠纤维肉瘤细胞在肿瘤坏死因子介导的细胞毒性中的存活率。
靶向非小细胞肺癌中SLC1a5介导的谷氨酰胺依赖性
Int J Cancer. 2015 Oct 1;137(7):1587-97. doi: 10.1002/ijc.29535. Epub 2015 May 6.
4
Bcl-xL silencing induces alterations in hsa-miR-608 expression and subsequent cell death in A549 and SK-LU1 human lung adenocarcinoma cells.Bcl-xL基因沉默会诱导人肺腺癌细胞A549和SK-LU1中hsa-miR-608表达的改变以及随后的细胞死亡。
PLoS One. 2013 Dec 10;8(12):e81735. doi: 10.1371/journal.pone.0081735. eCollection 2013.
5
Mer or Axl receptor tyrosine kinase inhibition promotes apoptosis, blocks growth and enhances chemosensitivity of human non-small cell lung cancer.-Mer 或 Axl 受体酪氨酸激酶抑制促进人非小细胞肺癌细胞凋亡,阻断生长并增强化疗敏感性。
Oncogene. 2013 Jul 18;32(29):3420-31. doi: 10.1038/onc.2012.355. Epub 2012 Aug 13.
6
Relevance of Bcl-x expression in different types of endometrial tissues.Bcl-x 表达与不同类型子宫内膜组织的相关性。
J Exp Clin Cancer Res. 2010 Feb 23;29(1):14. doi: 10.1186/1756-9966-29-14.
7
The pathobiology of splicing.剪接的病理生物学。
J Pathol. 2010 Jan;220(2):152-63. doi: 10.1002/path.2649.
8
Synergy between phosphatidylinositol 3-kinase/Akt pathway and Bcl-xL in the control of apoptosis in adenocarcinoma cells of the lung.磷脂酰肌醇3-激酶/蛋白激酶B信号通路与Bcl-xL在肺腺癌细胞凋亡调控中的协同作用
Mol Cancer Ther. 2009 Jan;8(1):101-9. doi: 10.1158/1535-7163.MCT-08-0973.
9
The role of oncogenes in drug resistance.癌基因在耐药性中的作用。
Cytotechnology. 1998 Sep;27(1-3):283-92. doi: 10.1023/A:1008053913764.
10
Growth suppression of lung cancer cells by targeting cyclic AMP response element-binding protein.通过靶向环磷酸腺苷反应元件结合蛋白抑制肺癌细胞生长
Cancer Res. 2008 Feb 15;68(4):981-8. doi: 10.1158/0008-5472.CAN-06-0249.
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4
Bcl-2 oncoprotein blocks chemotherapy-induced apoptosis in a human leukemia cell line.Bcl-2癌蛋白可阻断化疗诱导的人白血病细胞系凋亡。
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5
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6
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Cancer Res. 1993 Sep 15;53(18):4251-6.
7
bcl-2 protein in non-small-cell lung carcinoma.非小细胞肺癌中的bcl-2蛋白
N Engl J Med. 1993 Sep 2;329(10):690-4. doi: 10.1056/NEJM199309023291003.
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Bcl-2 proto-oncogene expression in Epstein-Barr-virus-associated nasopharyngeal carcinoma.Bcl-2原癌基因在爱泼斯坦-巴尔病毒相关鼻咽癌中的表达。
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9
Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death.Bcl-2在体内与一个保守的同源物Bax形成异二聚体,后者会加速程序性细胞死亡。
Cell. 1993 Aug 27;74(4):609-19. doi: 10.1016/0092-8674(93)90509-o.
10
bcl-x, a bcl-2-related gene that functions as a dominant regulator of apoptotic cell death.bcl-x,一种与bcl-2相关的基因,作为凋亡细胞死亡的主要调节因子发挥作用。
Cell. 1993 Aug 27;74(4):597-608. doi: 10.1016/0092-8674(93)90508-n.