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Targeted Cancer Therapies02:57

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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
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Cell Death Associated with Abnormal Mitosis Observed by Confocal Imaging in Live Cancer Cells
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Cell Death Associated with Abnormal Mitosis Observed by Confocal Imaging in Live Cancer Cells

Published on: August 21, 2013

Killing cells by targeting mitosis.

E Manchado1, M Guillamot, M Malumbres

  • 1Cell Division and Cancer Group, Spanish National Cancer Research Center, Madrid, Spain.

Cell Death and Differentiation
|January 7, 2012
PubMed
Summary
This summary is machine-generated.

Targeting cancer cell division, particularly mitosis, offers promising therapeutic strategies. Inhibiting mitotic exit shows potential for inducing cancer cell death, advancing new clinical treatments.

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Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
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Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics

Published on: May 14, 2016

Area of Science:

  • Oncology
  • Cell Biology
  • Cancer Therapeutics

Background:

  • Cell cycle deregulation and genomic instability are hallmarks of human cancers.
  • Targeting cancer cell proliferation is a key therapeutic strategy.
  • Mitosis offers multiple targets for cancer cell killing.

Purpose of the Study:

  • To review current therapeutic strategies targeting the cell division cycle in cancer.
  • To explore novel approaches focusing on mitosis and mitotic exit.
  • To highlight the potential of targeting mitotic pathways for cancer treatment.

Main Methods:

  • Review of existing literature on cell cycle targeting in cancer.
  • Analysis of novel strategies including kinase inhibitors and checkpoint abrogation.
  • Examination of targeting mitotic exit via anaphase-promoting complex inhibition.

Main Results:

  • Inhibiting initial cell cycle phases may yield quiescent cells, while targeting mitosis offers cell death possibilities.
  • Microtubule poisons are clinically effective; novel targets include kinases and kinesins.
  • Inhibiting mitotic exit induces metaphase cell death, suggesting a potent therapeutic window.

Conclusions:

  • Targeting mitosis, especially mitotic exit, presents a promising strategy for cancer therapy.
  • Further research into molecular pathways of mitotic cell death is crucial for clinical translation.
  • Novel approaches like anaphase-promoting complex inhibition warrant clinical investigation.