Cytotoxic effect and apoptotic induction of tricyclohexyltin p-methoxycinnamate on HT-29 colorectal cancer cells: Implications for anticancer therapeutics

Colorectal cancer’s escalating prevalence in Malaysia prompts the exploration of innovative anticancer agents; amidst this backdrop, tricyclohexyltin p-methoxycinnamate emerges as a synthesized organotin complex with unique bioactive properties. Notably, the novelty of this research lies in its grou...

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Main Authors: Abdah Md Akim, Gul-e-Saba Chaudhry, Zeenia, Tan Weay Ken, Yeong Yik Sung, Tengku Sifzizul Tengku Muhammad
Format: Article
Jezik:English
Izdano: Wolters Kluwer Medknow Publications 2025-01-01
Serija:Journal of Advanced Pharmaceutical Technology & Research
Teme:
Online dostop:https://journals.lww.com/10.4103/JAPTR.JAPTR_427_23
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author Abdah Md Akim
Gul-e-Saba Chaudhry
Zeenia
Tan Weay Ken
Yeong Yik Sung
Tengku Sifzizul Tengku Muhammad
author_facet Abdah Md Akim
Gul-e-Saba Chaudhry
Zeenia
Tan Weay Ken
Yeong Yik Sung
Tengku Sifzizul Tengku Muhammad
author_sort Abdah Md Akim
collection DOAJ
description Colorectal cancer’s escalating prevalence in Malaysia prompts the exploration of innovative anticancer agents; amidst this backdrop, tricyclohexyltin p-methoxycinnamate emerges as a synthesized organotin complex with unique bioactive properties. Notably, the novelty of this research lies in its groundbreaking investigation into the hitherto unexplored anticancer potential and mode of cell death induced by tricyclohexyltin p-methoxycinnamate on colon cancer (human colorectal adenocarcinoma cell line (HT-29)) cell lines. This study pioneers the assessment of tricyclohexyltin p-methoxycinnamate’s cytotoxic effects through the “(3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) assay,” revealing a dose- and time-dependent cytotoxicity with IC50 values of 1.2 × 10-6M for 24 h, 1.0 × 10-6M for 48 h, and 5.0 × 10-7M for 72 h. The mode of cell death through “AO/PI” staining alongside cell cycle analysis, highlighting apoptosis as the predominant mode of cell death in the HT-29 cell line, accompanied by substantial cell cycle arrest at the sub-“G0” phase. The tricyclohexyltin p-methoxycinnamate’s shown potential antiproliferative properties, cell cycle arrest, and apoptosis in HT-29 cancer cells. This novel insight into the compound’s mode of action positions it as a promising candidate for future anticancer therapeutics. The study underscores the urgency of investigating innovative approaches amidst the rising colorectal cancer rates, emphasizing the compound’s potential through further in-depth studies and preclinical trials.
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spelling doaj.art-f57f75bff4b6421cad646d28d1dc8a6a2025-03-06T09:38:29ZengWolters Kluwer Medknow PublicationsJournal of Advanced Pharmaceutical Technology & Research2231-40400976-20942025-01-011611510.4103/JAPTR.JAPTR_427_23Cytotoxic effect and apoptotic induction of tricyclohexyltin p-methoxycinnamate on HT-29 colorectal cancer cells: Implications for anticancer therapeuticsAbdah Md AkimGul-e-Saba ChaudhryZeeniaTan Weay KenYeong Yik SungTengku Sifzizul Tengku MuhammadColorectal cancer’s escalating prevalence in Malaysia prompts the exploration of innovative anticancer agents; amidst this backdrop, tricyclohexyltin p-methoxycinnamate emerges as a synthesized organotin complex with unique bioactive properties. Notably, the novelty of this research lies in its groundbreaking investigation into the hitherto unexplored anticancer potential and mode of cell death induced by tricyclohexyltin p-methoxycinnamate on colon cancer (human colorectal adenocarcinoma cell line (HT-29)) cell lines. This study pioneers the assessment of tricyclohexyltin p-methoxycinnamate’s cytotoxic effects through the “(3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) assay,” revealing a dose- and time-dependent cytotoxicity with IC50 values of 1.2 × 10-6M for 24 h, 1.0 × 10-6M for 48 h, and 5.0 × 10-7M for 72 h. The mode of cell death through “AO/PI” staining alongside cell cycle analysis, highlighting apoptosis as the predominant mode of cell death in the HT-29 cell line, accompanied by substantial cell cycle arrest at the sub-“G0” phase. The tricyclohexyltin p-methoxycinnamate’s shown potential antiproliferative properties, cell cycle arrest, and apoptosis in HT-29 cancer cells. This novel insight into the compound’s mode of action positions it as a promising candidate for future anticancer therapeutics. The study underscores the urgency of investigating innovative approaches amidst the rising colorectal cancer rates, emphasizing the compound’s potential through further in-depth studies and preclinical trials.https://journals.lww.com/10.4103/JAPTR.JAPTR_427_23anticancerapoptosiscancercell cycletricyclohexyltin p-methoxycinnamate
spellingShingle Abdah Md Akim
Gul-e-Saba Chaudhry
Zeenia
Tan Weay Ken
Yeong Yik Sung
Tengku Sifzizul Tengku Muhammad
Cytotoxic effect and apoptotic induction of tricyclohexyltin p-methoxycinnamate on HT-29 colorectal cancer cells: Implications for anticancer therapeutics
Journal of Advanced Pharmaceutical Technology & Research
anticancer
apoptosis
cancer
cell cycle
tricyclohexyltin p-methoxycinnamate
title Cytotoxic effect and apoptotic induction of tricyclohexyltin p-methoxycinnamate on HT-29 colorectal cancer cells: Implications for anticancer therapeutics
title_full Cytotoxic effect and apoptotic induction of tricyclohexyltin p-methoxycinnamate on HT-29 colorectal cancer cells: Implications for anticancer therapeutics
title_fullStr Cytotoxic effect and apoptotic induction of tricyclohexyltin p-methoxycinnamate on HT-29 colorectal cancer cells: Implications for anticancer therapeutics
title_full_unstemmed Cytotoxic effect and apoptotic induction of tricyclohexyltin p-methoxycinnamate on HT-29 colorectal cancer cells: Implications for anticancer therapeutics
title_short Cytotoxic effect and apoptotic induction of tricyclohexyltin p-methoxycinnamate on HT-29 colorectal cancer cells: Implications for anticancer therapeutics
title_sort cytotoxic effect and apoptotic induction of tricyclohexyltin p methoxycinnamate on ht 29 colorectal cancer cells implications for anticancer therapeutics
topic anticancer
apoptosis
cancer
cell cycle
tricyclohexyltin p-methoxycinnamate
url https://journals.lww.com/10.4103/JAPTR.JAPTR_427_23
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AT zeenia cytotoxiceffectandapoptoticinductionoftricyclohexyltinpmethoxycinnamateonht29colorectalcancercellsimplicationsforanticancertherapeutics
AT tanweayken cytotoxiceffectandapoptoticinductionoftricyclohexyltinpmethoxycinnamateonht29colorectalcancercellsimplicationsforanticancertherapeutics
AT yeongyiksung cytotoxiceffectandapoptoticinductionoftricyclohexyltinpmethoxycinnamateonht29colorectalcancercellsimplicationsforanticancertherapeutics
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