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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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Cancer treatment vaccines are a rapidly evolving field that offers a promising approach to immunotherapy. Unlike traditional vaccines that prevent diseases, cancer treatment vaccines are designed to treat existing cancers by stimulating the immune system to recognize and attack cancer cells.
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Updated: Oct 18, 2025

Author Spotlight: Exploring Salidroside's Molecular Mechanisms in Breast Cancer Treatment
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Vorinostat (SAHA) and Breast Cancer: An Overview.

Anna Wawruszak1, Lidia Borkiewicz1, Estera Okon1

  • 1Department of Biochemistry and Molecular Biology, Medical University of Lublin, 20-093 Lublin, Poland.

Cancers
|September 28, 2021
PubMed
Summary

Vorinostat (SAHA), a histone deacetylase inhibitor, shows promise in treating breast carcinoma (BC) by inhibiting cancer cell proliferation. This review analyzes SAHA

Keywords:
breast cancerepigeneticshistone acetylationhistone deacetylase inhibitor (HDI)histone deacetylases (HDACs)suberoylanilide hydroxamic acidtargeted therapyvorinostat (SAHA)

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Area of Science:

  • Oncology
  • Pharmacology
  • Molecular Biology

Background:

  • Histone deacetylase inhibitors (HDIs) are emerging anticancer agents.
  • Vorinostat (SAHA) is the first approved HDI for cutaneous T-cell lymphoma.
  • Breast carcinoma (BC) presents therapeutic challenges due to heterogeneity, toxicity, and drug resistance.

Purpose of the Study:

  • To analyze preclinical and clinical data on Vorinostat (SAHA) for breast carcinoma treatment.
  • To evaluate SAHA's efficacy as a single agent and in combination therapies.
  • To consider the impact of different BC histological subtypes on SAHA's effectiveness.

Main Methods:

  • Systematic review of preclinical studies.
  • Analysis of clinical trial data.
  • Evaluation of SAHA in various breast carcinoma models and patient cohorts.

Main Results:

  • SAHA demonstrates antiproliferative effects across various cancer cell types, including breast carcinoma.
  • Combination therapies involving SAHA show potential for enhanced efficacy.
  • Response to SAHA may vary depending on the specific histological subtype of breast carcinoma.

Conclusions:

  • Vorinostat (SAHA) is a promising agent for breast carcinoma treatment, warranting further investigation.
  • Combination strategies with SAHA could overcome resistance and reduce toxicity.
  • Tailoring SAHA-based therapy to BC subtypes may improve patient outcomes.