Evidence map›Paper›PMID 39733438›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2024

Proteomic Analysis of Anticancer Effect of Myo-inositol in Human Prostate Cancer (DU-145) Cell Line.

Mohammad Jahidul Islam, Sidratul Muntaha, Md Mohiuddin Masum, Sazia Nowshin, Sabia Salam, Mominul Haque, Myo Wint Zaw, Shahriar Jahan

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Article in Asian Pacific journal of cancer prevention : APJCP, 2024. 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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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Mohammad Jahidul IslamDepartment of Pharmacology. Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.ORCID 0000-0003-1232-6799
Sidratul MuntahaDepartment of Biochemistry, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.ORCID 0009-0005-3988-387X
Md Mohiuddin MasumDepartment of Anatomy, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.ORCID 0000-0001-5103-6933
Sazia NowshinDepartment of Surveillance & Immunization, World health organization (WHO), Dhaka. Bangladesh.ORCID 0009-0004-1328-1398
Sabia SalamNational Institute of Ophthalmology & Hospital, Dhaka, Bangladesh.ORCID 0009-0006-3457-3992
Mominul HaqueDepartment of Anatomy, Popular Medical College, Dhaka, Bangladesh.
Myo Wint ZawDepartment of Biochemistry, University of Cyberjaya, Malaysia.
Shahriar JahanDepartment of Molecular Biology, EW Villa Medica, Dhaka, Bangladesh.ORCID 0000-0002-9351-8604

Funding

World Health Organization 001
6 · The paper itself

Abstract

objectiveThis study investigated the potential anticancer properties of Myo-inositol on the DU-145 prostate cancer cell line.

methodsThe DU-145 cells have been treated to different doses of Myo-inositol in order to ascertain the half-maximal inhibitory concentration (IC50) using the trypan blue exclusion assay. The impact of Myo-inositol on proteomic profiles was evaluated using 2D gel electrophoresis and liquid chromatography-mass spectrometry (LC-MS).

resultsMyo-inositol significantly reduced DU-145 cell viability with an IC50 of 0.06 mg/ml (p<0.05). Proteomic analysis highlighted marked differences in protein expression between treated and untreated cells, particularly in proteins related to cytoskeletal regulation, apoptosis, and stress response. LC-MS further identified significant alterations in protein profiles, with suppression of proteins like Annexin A2 and Cofilin-1-A in controls, and upregulation of proteins such as Rho GTPase-activating protein, Apoptotic protease-activating factor 1 (APAF1), and TNF receptor-associated factor 2 (TRAF2) in treated samples (p<0.001), indicating modulation of key signaling pathways involved in tumor suppression and oncogenesis.

conclusionMyo-inositol exhibits anticancer properties in prostate cancer cells by impacting cell viability and altering protein expression. While promising as an adjunctive treatment, further studies are needed to understand its mechanisms and potential in combination therapies for managing CRPC.

Indexed as

ApoptosisInositolProstatic NeoplasmsProteomicsAnnexin A2Antineoplastic AgentsCell Line, TumorCell ProliferationCell SurvivalCofilin 1HumansMaleTumor Cells, CulturedAnnexin A2Antineoplastic AgentsANXA2 protein, humanCofilin 1InositolHuman prostate cancer (DU-145) cell lineKey words: Proteomic analysisMyo-inositol

Identifiers

PMID39733438
PMCPMC12008332

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