The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
The role of Bcl-2 and its pro-survival relatives in tumourigenesis and cancer therapy
Open accessAbstract
Tumour development requires a combination of defects that allow nascent neoplastic cells to become self-sufficient for cell proliferation and insensitive to signals that normally restrain cell growth. Among the latter, evasion of programmed cell death (apoptosis) has proven to be critical for the development and sustained growth of many, perhaps all, cancers. Apoptotic cell death is regulated by complex interactions between pro-survival members and two subgroups of pro-apoptotic members of the B-cell lymphoma-2 (Bcl-2) protein family. In this invited review article, we reminisce on the discovery of Bcl-2, the first regulator of cell death identified, we discuss the mechanisms that control apoptotic cell death, focussing on how defects in this process promote the development and sustained growth of tumours and also affect their responses to anticancer therapeutics and, finally, we describe how current knowledge of the regulatory networks of apoptosis is exploited to develop novel approaches for cancer therapy.
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The role of BCL-2 family proteins in regulating apoptosis and cancer therapy
Qian, S., Wei, Z., Yang, W., Huang, J., Yang, Y., & Wang, J. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.985363 · Cited by 1,011
The BCL2 Family: Key Mediators of the Apoptotic Response to Targeted Anticancer Therapeutics
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Sharma, A., Singh, K., Mazumder, S., Hill, B. T., Kalaycio, M., & Almasan, A. (2013) · Cell Death & Disease · doi:10.1038/cddis.2013.155 · Cited by 39
Phenylpropanoids, eugenol scaffold, and its derivatives as anticancer
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Overcoming Resistance to AC0010, a Third Generation of EGFR Inhibitor, by Targeting c-MET and BCL-2
Xu, W., Tang, W., Li, T., Zhang, X., & Sun, Y. (2019) · Neoplasia · doi:10.1016/j.neo.2018.11.004 · Cited by 23
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Metadata
- Authors
- Kelly, P. N., & Strasser, A.
- Venue
- Cell Death & Differentiation
- Published
- 2011-03-18
- Volume
- 18
- Issue
- 9
- Pages
- 1414-1424
- ISSN
- 1350-9047 (ISSN-L)
- 1476-5403
- OpenAlex
- W2018439544
- Cited by
- 453
- References
- 9
- FWCI
- 19.98
- Type
- journal article
- Language
- en
- Open access
- bronze
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