Abstract:
:Chemotherapeutic targeting of microtubules has been the standard of care in treating a variety of malignancies for decades. During mitosis, increased microtubule dynamics are necessary for mitotic spindle formation and successful chromosomal segregation. Microtubule targeting agents (MTAs) disrupt the dynamics necessary for successful spindle assembly and trigger programmed cell death (apoptosis). As the critical regulators of apoptosis, anti-apoptotic BCL2 family members are often amplified during carcinogenesis that can result in MTA resistance. This review outlines how BCL2 family regulation is positioned within the context of MTA treatment and explores the potential of combination therapy of MTAs with emerging BCL2 family inhibitors.
journal_name
Cellsjournal_title
Cellsauthors
Whitaker RH,Placzek WJdoi
10.3390/cells8040346subject
Has Abstractpub_date
2019-04-12 00:00:00issue
4issn
2073-4409pii
cells8040346journal_volume
8pub_type
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