Evidence map›Paper›PMID 41459864›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2025

Curcumin Enhanced the Chemosensitivity of Breast Cancer Cells through the Intrinsic Pathway of Apoptosis.

Zahra Sadat Miri, Hossein Bagheri, Alireza Amani, Hadi Karami

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Article in Asian Pacific journal of cancer prevention : APJCP, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Zahra Sadat MiriMolecular and Medicine Research Center, Arak University of Medical Sciences, Arak, Iran.
Hossein BagheriDepartment of Applied Cell Sciences, Faculty of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Alireza AmaniDepartment of Orthopedic, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran.
Hadi KaramiDepartment of Molecular Medicine and Biotechnology, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOver-expression of the anti-apoptotic proteins like Mcl-1 is linked to the development of resistance in tumor cells against the Bcl-2 inhibitor ABT- 737. Combination therapy involving Bcl-2 inhibitors and Mcl-1 inhibitors has been suggested as a promising approach to address the issue of drug resistance. In this study, we examined the impact of curcumin on the expression of Mcl-1 and the sensitivity MDA-MB-231 and MCF-7 breast cancer cells to ABT-737.

methodsIn this experimental study, cell toxicity was evaluated using MTT assay. The cell growth assay and colony formation assay were used to evaluate the effect of treatments on cell proliferation. The mRNA levels of Mcl-1 and MMP-2 were determined by qRT-PCR. Cell migration was assessed by wound healing assay. Apoptosis was detected by Hoechst 33342 staining, ELISA cell death assay and caspase-3 activity assay.

resultsOur data demonstrated that combination treatment with curcumin and ABT-737 synergistically lowered the IC50 values and reduced colony formation, cell migration, and cell survival compared with curcumin or ABT-737 alone. ABT-737 increased the expression level of Mcl-1 mRNA, while curcumin suppressed the expression of both Mcl-1 and MMP-2 mRNA. Moreover, suppression of Mcl-1 expression by curcumin was associated with enhanced apoptosis induced by ABT-737 in breast cancer cells.

conclusionIn conclusion, curcumin demonstrates anti-tumor activity in human breast cancer cells by inhibiting colony formation, cell migration, and cell survival. Furthermore, curcumin can augment the apoptotic effect of ABT-737 by suppressing the expression of Mcl-1.

Indexed as

ApoptosisBreast NeoplasmsCurcuminDrug Resistance, NeoplasmAntineoplastic AgentsBiphenyl CompoundsCell MovementCell ProliferationDrug SynergismFemaleHumansMatrix Metalloproteinase 2Myeloid Cell Leukemia Sequence 1 ProteinNitrophenolsPiperazinesProto-Oncogene Proteins c-bcl-2ABT-737Antineoplastic AgentsBiphenyl CompoundsCurcuminMatrix Metalloproteinase 2MCL1 protein, humanMyeloid Cell Leukemia Sequence 1 ProteinNitrophenolsPiperazinesProto-Oncogene Proteins c-bcl-2SulfonamidesABT-737Apoptosisbreast cancercurcuminMcl-1

Identifiers

PMID41459864
PMCPMC13242557

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