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Endocr Relat Cancer. 2017 Sep;24(9):T65-T82. doi: 10.1530/ERC-17-0080. Epub 2017 Jun 14.

Targeting mitotic pathways for endocrine-related cancer therapeutics.

Author information

1
Department of Cell and Molecular BiologyFeinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
2
Department of Cell and Molecular BiologyFeinberg School of Medicine, Northwestern University, Chicago, Illinois, USA dileep.varma@northwestern.edu.

Abstract

A colossal amount of basic research over the past few decades has provided unprecedented insights into the highly complex process of cell division. There is an ever-expanding catalog of proteins that orchestrate, participate and coordinate in the exquisite processes of spindle formation, chromosome dynamics and the formation and regulation of kinetochore microtubule attachments. Use of classical microtubule poisons has still been widely and often successfully used to combat a variety of cancers, but their non-selective interference in other crucial physiologic processes necessitate the identification of novel druggable components specific to the cell cycle/division pathway. Considering cell cycle deregulation, unscheduled proliferation, genomic instability and chromosomal instability as a hallmark of tumor cells, there lies an enormous untapped terrain that needs to be unearthed before a drug can pave its way from bench to bedside. This review attempts to systematically summarize the advances made in this context so far with an emphasis on endocrine-related cancers and the avenues for future progress to target mitotic mechanisms in an effort to combat these dreadful cancers.

KEYWORDS:

cancer; endocrine; kinetochores; microtubules; mitosis; spindle; therapeutics

PMID:
28615236
PMCID:
PMC5557717
DOI:
10.1530/ERC-17-0080
[Indexed for MEDLINE]
Free PMC Article

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