• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

BCL2:一种有前途的癌症治疗靶点。

BCL2: A promising cancer therapeutic target.

机构信息

Department of Biochemistry, Indian Institute of Science, Bangalore 560012, India.

Department of Biochemistry, Indian Institute of Science, Bangalore 560012, India.

出版信息

Biochim Biophys Acta Rev Cancer. 2017 Aug;1868(1):309-314. doi: 10.1016/j.bbcan.2017.06.004. Epub 2017 Jun 21.

DOI:10.1016/j.bbcan.2017.06.004
PMID:28647470
Abstract

A remarkable characteristic of majority of cancer cells is that, they fail to undergo apoptosis, which in turn confers them a survival advantage over normal cells. Targeted cancer therapy aims at disrupting the functions of proteins that play an important role during cancer progression. Antiapoptotic protein, BCL2, is one such protein that is highly upregulated in many cancers as compared to normal cells, making it an ideal target for cancer therapy. Although, several BCL2 targeting agents have been investigated over the past 30 years, very few have exhibited any clinical significance. This mini-review outlines a road map of existing BCL2 inhibitors and their relevance in treating cancer, and discusses potential strategies for future research with respect to BCL2 specific cancer therapy.

摘要

大多数癌细胞的一个显著特征是,它们无法进行细胞凋亡,这使它们相对于正常细胞具有生存优势。靶向癌症治疗旨在破坏在癌症进展过程中发挥重要作用的蛋白质的功能。抗凋亡蛋白 BCL2 就是这样一种蛋白质,与正常细胞相比,它在许多癌症中高度上调,使其成为癌症治疗的理想靶点。尽管过去 30 年来已经研究了几种 BCL2 靶向药物,但很少有药物表现出任何临床意义。这篇迷你综述概述了现有的 BCL2 抑制剂及其在治疗癌症方面的相关性,并讨论了针对 BCL2 特异性癌症治疗的未来研究的潜在策略。

相似文献

1
BCL2: A promising cancer therapeutic target.BCL2:一种有前途的癌症治疗靶点。
Biochim Biophys Acta Rev Cancer. 2017 Aug;1868(1):309-314. doi: 10.1016/j.bbcan.2017.06.004. Epub 2017 Jun 21.
2
Tumor suppressor miRNA-204-5p promotes apoptosis by targeting BCL2 in prostate cancer cells.抑癌 miRNA-204-5p 通过靶向前列腺癌细胞中的 BCL2 促进细胞凋亡。
Asian J Surg. 2017 Sep;40(5):396-406. doi: 10.1016/j.asjsur.2016.07.001. Epub 2016 Aug 9.
3
The BCL2 Family: Key Mediators of the Apoptotic Response to Targeted Anticancer Therapeutics.BCL2家族:靶向抗癌治疗凋亡反应的关键调节因子
Cancer Discov. 2015 May;5(5):475-87. doi: 10.1158/2159-8290.CD-15-0011. Epub 2015 Apr 20.
4
Endoplasmic reticulum targeted Bcl2 confers long term cell survival through phosphorylation of heat shock protein 27.内质网靶向 Bcl2 通过磷酸化热休克蛋白 27 赋予细胞长期存活能力。
Int J Biochem Cell Biol. 2010 Dec;42(12):1984-92. doi: 10.1016/j.biocel.2010.08.011. Epub 2010 Aug 26.
5
Novel BCL2 inhibitor, Disarib induces apoptosis by disruption of BCL2-BAK interaction.新型BCL2抑制剂Disarib通过破坏BCL2与BAK的相互作用诱导细胞凋亡。
Biochem Pharmacol. 2017 May 1;131:16-28. doi: 10.1016/j.bcp.2017.02.015. Epub 2017 Feb 20.
6
A novel inhibitor of BCL2, Disarib abrogates tumor growth while sparing platelets, by activating intrinsic pathway of apoptosis.一种新型的BCL2抑制剂Disarib,通过激活细胞凋亡的内在途径,在不影响血小板的情况下消除肿瘤生长。
Biochem Pharmacol. 2016 Dec 15;122:10-22. doi: 10.1016/j.bcp.2016.09.028. Epub 2016 Sep 29.
7
Reprogramming cell death: BCL2 family inhibition in hematological malignancies.重编程细胞死亡:血液系统恶性肿瘤中 BCL2 家族抑制。
Immunol Lett. 2013 Sep-Oct;155(1-2):36-9. doi: 10.1016/j.imlet.2013.09.015. Epub 2013 Oct 1.
8
Molecular profile of the BCL2 family of the apoptosis related genes in breast cancer cells after treatment with cytotoxic/cytostatic drugs.细胞毒性/细胞抑制药物处理后乳腺癌细胞中凋亡相关基因BCL2家族的分子特征
Connect Tissue Res. 2008;49(3):261-4. doi: 10.1080/03008200802147829.
9
Apoptosis-related BCL2-family members: Key players in chemotherapy.凋亡相关的 BCL2 家族成员:化疗中的关键角色。
Anticancer Agents Med Chem. 2014 Mar;14(3):353-74. doi: 10.2174/18715206113139990091.
10
AMBRA1, a Novel BH3-Like Protein: New Insights Into the AMBRA1-BCL2-Family Proteins Relationship.AMBRA1,一种新型的类BH3蛋白:对AMBRA1与BCL2家族蛋白关系的新见解。
Int Rev Cell Mol Biol. 2017;330:85-113. doi: 10.1016/bs.ircmb.2016.09.002. Epub 2016 Nov 15.

引用本文的文献

1
Latest Advancements of Natural Products in Combating Ovarian Cancer.天然产物在对抗卵巢癌方面的最新进展
J Cancer. 2025 Jul 28;16(11):3497-3512. doi: 10.7150/jca.118209. eCollection 2025.
2
Regulatory Functions of microRNAs in Cancer Stem Cells: Mechanism, Facts, and Perspectives.微小RNA在癌症干细胞中的调控功能:机制、事实与展望
Cells. 2025 Jul 14;14(14):1073. doi: 10.3390/cells14141073.
3
Immunohistochemical profiling of Bcl-2 and EGFR proteins in cervical carcinoma at a tertiary hospital in Ghana.加纳一家三级医院宫颈癌中Bcl-2和表皮生长因子受体(EGFR)蛋白的免疫组织化学分析
Niger Med J. 2025 Jun 16;66(2):575-585. doi: 10.71480/nmj.v66i2.713. eCollection 2025 Mar-Apr.
4
Mechanism of Action and Efficacy of Wu-Hua-Yan-Xiao in the Treatment of Pediatric Acute Pharyngitis Based on Network Pharmacology and Experimental Validation.基于网络药理学和实验验证的五华咽炎消治疗小儿急性咽炎的作用机制及疗效
Drug Des Devel Ther. 2025 May 24;19:4321-4342. doi: 10.2147/DDDT.S513073. eCollection 2025.
5
Deciphering the effects of bixin on pulmonary alveolar adenocarcinoma migration and proliferation via targeting BAX/BCL-2 and Cyclin D1.通过靶向BAX/BCL-2和细胞周期蛋白D1来解读胭脂树素对肺泡腺癌迁移和增殖的影响。
Sci Rep. 2025 Apr 29;15(1):15109. doi: 10.1038/s41598-025-96788-9.
6
TFF3 facilitates dormancy of anti-estrogen treated ER+ mammary carcinoma.三叶因子3(TFF3)促进抗雌激素治疗的雌激素受体阳性(ER+)乳腺癌的休眠。
Commun Med (Lond). 2025 Feb 21;5(1):45. doi: 10.1038/s43856-024-00710-9.
7
Microrna-342 inhibits hepatocellular carcinoma cell proliferation and promotes apoptosis through the FOXP1/MYCBP Signaling Axis.微小RNA-342通过FOXP1/MYCBP信号轴抑制肝癌细胞增殖并促进细胞凋亡。
Toxicol Res (Camb). 2024 Dec 17;13(6):tfae149. doi: 10.1093/toxres/tfae149. eCollection 2024 Dec.
8
Trace elements and metal nanoparticles: mechanistic approaches to mitigating chemotherapy-induced toxicity-a review of literature evidence.微量元素与金属纳米颗粒:减轻化疗诱导毒性的机制研究方法——文献证据综述
Biometals. 2024 Dec;37(6):1325-1378. doi: 10.1007/s10534-024-00637-7. Epub 2024 Sep 30.
9
Advancing Breast Cancer Therapeutics: Targeted Gene Delivery Systems Unveiling the Potential of Estrogen Receptor-Targeting Ligands.推进乳腺癌治疗:靶向基因递送系统揭示雌激素受体靶向配体的潜力。
Biomater Res. 2024 Sep 24;28:0087. doi: 10.34133/bmr.0087. eCollection 2024.
10
Effect of venom (AAVC-I) on apoptosis through modulation of the Keap1/Nrf2 pathway in HSC-3 oral squamous cell carcinoma cells.毒液(AAVC-I)通过调节Keap1/Nrf2通路对HSC-3口腔鳞状细胞癌细胞凋亡的影响。
Transl Cancer Res. 2024 Aug 31;13(8):4341-4353. doi: 10.21037/tcr-24-182. Epub 2024 Aug 17.