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Anti-Cancer Activity of Curcumin on Multiple Myeloma.

  • H. Mirzaei
  • , H. Bagheri
  • , F. Ghasemi
  • , J.M. Khoi
  • , M.H. Pourhanifeh
  • , Yvan Vander Heyden
  • , E. Mortezapour
  • , A. Nikdasti
  • , P. Jeandet
  • , H. Khan
  • , A. Sahebkar

Research output: Contribution to journalArticlepeer-review

40 Citations (Scopus)

Abstract

Multiple Myeloma (MM) is the third most common and deadly hematological malignancy, which is characterized by a progressive monoclonal proliferation within the bone marrow. MM is cytogenetically hetero-geneous with numerous genetic and epigenetic alterations, which lead to a wide spectrum of signaling pathways and cell cycle checkpoint aberrations. MM symptoms can be attributed to CRAB features (hyperCalcemia, Re-nal failure, Anemia, and Bone lesion), which profoundly affect both the Health-Related Quality of Life (HRQoL) and the life expectancy of patients. Despite all enhancement and improvement in therapeutic strate-gies, MM is almost incurable, and patients suffering from this disease eventually relapse. Curcumin is an active and non-toxic phenolic compound, isolated from the rhizome of Curcuma longa L. It has been widely studied and has a confirmed broad range of therapeutic properties, especially anti-cancer activity, and others, including anti-proliferation, anti-angiogenesis, antioxidant and anti-mutation activities. Curcumin induces apoptosis in cancerous cells and prevents Multidrug Resistance (MDR). Growing evidence concerning the therapeutic properties of curcumin caused a pharmacological impact on MM. It is confirmed that curcumin interferes with vari-ous signaling pathways and cell cycle checkpoints, and with oncogenes. In this paper, we summarized the anti-MM effects of curcumin.

Original languageEnglish
Pages (from-to)575-586
Number of pages12
JournalAnti-Cancer Agents in Medicinal Chemistry
Volume21
Issue number5
DOIs
Publication statusPublished - 1 Jan 2021

Keywords

  • CRAB features.; Curcumin; HRQoL; multidrug resistance; multiple myeloma; therapy.

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