Contribution of non-steroidal anti-inflammatory drugs to breast cancer treatment: and studies.

Vet World

Centre for the Research and Technology of Agro-Environmental and Biological Sciences (CITAB), University of Trás-os-Montes and Alto Douro, 5000-801 Vila Real, Portugal.

Published: May 2024

AI Article Synopsis

  • Chronic inflammation is linked to cancer development, with high levels of prostaglandin E2 and COX-2 expression identified in several types of cancer, impacting tumor growth and immune response.
  • Non-steroidal anti-inflammatory drugs (NSAIDs) are used to lower pain and inflammation by blocking COX-2, which could have implications for cancer treatment.
  • This review discusses how NSAIDs and COX-2 inhibitors might be utilized for breast cancer therapy, based on various laboratory studies assessing their effectiveness and potential use alongside other cancer treatments.

Article Abstract

Chronic inflammation plays a crucial role in carcinogenesis. High levels of serum prostaglandin E2 and tissue overexpression of cyclooxygenase-2 (COX-2) have been described in breast, urinary, colorectal, prostate, and lung cancers as being involved in tumor initiation, promotion, progression, angiogenesis, and immunosuppression. Non-steroidal anti-inflammatory drugs (NSAIDs) are prescribed for several medical conditions to not only decrease pain and fever but also reduce inflammation by inhibiting COX and its product synthesis. To date, significant efforts have been made to better understand and clarify the interplay between cancer development, inflammation, and NSAIDs with a view toward addressing their potential for cancer management. This review provides readers with an overview of the potential use of NSAIDs and selective COX-2 inhibitors for breast cancer treatment, highlighting pre-clinical in vitro and in vivo studies employed to evaluate the efficacy of NSAIDs and their use in combination with other antineoplastic drugs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11188899PMC
http://dx.doi.org/10.14202/vetworld.2024.1052-1072DOI Listing

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