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Ganoderma lucidum put forth anti-tumor activity against PC-3 prostate cancer cells via inhibition of Jak-1/STAT-3 activity

BACKGROUND: Prostate cancer (PCA) is a frequent cancer that mainly affects the men. Studying growth feature pathways modified during PCA development may facilitate researchers to expand embattled therapeutic strategies for prostate cancer. In present study, we examined the anticancer potentials of G...

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Autores principales: Wang, Xiaoming, Wang, Bo, Zhou, Liquan, Wang, Xiang, Veeraraghavan, Vishnu Priya, Mohan, Surapaneni Krishna, Xin, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499110/
https://www.ncbi.nlm.nih.gov/pubmed/32994721
http://dx.doi.org/10.1016/j.sjbs.2020.05.044
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author Wang, Xiaoming
Wang, Bo
Zhou, Liquan
Wang, Xiang
Veeraraghavan, Vishnu Priya
Mohan, Surapaneni Krishna
Xin, Feng
author_facet Wang, Xiaoming
Wang, Bo
Zhou, Liquan
Wang, Xiang
Veeraraghavan, Vishnu Priya
Mohan, Surapaneni Krishna
Xin, Feng
author_sort Wang, Xiaoming
collection PubMed
description BACKGROUND: Prostate cancer (PCA) is a frequent cancer that mainly affects the men. Studying growth feature pathways modified during PCA development may facilitate researchers to expand embattled therapeutic strategies for prostate cancer. In present study, we examined the anticancer potentials of Ganoderma lucidum against the prostate cancer (PC-3) cells by inflection of JAK-1/STAT-3 signalling pathway. METHODS: The cytotoxicity of G. lucidum against the PC-3 cells was examined by MTT assay. The ROS production was monitored by using DCFH-DA staining. The apoptotic morphological alterations stimulatory potential of G. lucidum on PC-3 cells was inspected through the dual staining. The expression of Bcl-2, JAK-1, STAT3, Bax and CyclinD1 proteins were measured by western blotting. The caspase-3 and 9 functions were condensed by assay kit. RESULTS: Findings demonstrates the Ganoderma lucidum convince cytotoxicity, accretion of ROS, and apoptosis stimulation in PC-3 cells. In addition, signal transducer and activating transcription (STAT-3) is a successive oncogenic transcriptional factor that regularizes multiplication and apoptosis in cells. Discretion of STAT-3 transcription deliberated as original approach to hinder prostate cell growth. In present exploration, we ascertain that Ganoderma lucidum hold back STAT-3 translocation, in that way dropping the eminent expression of, BCL-2, cyclin-D1 and declined the Bax, caspase-3 and 9 expressions in PC-3 cells. CONCLUSION: In the end our finding concluded that Ganoderma lucidum hinder prostate cell development and convinces apoptosis via hampering the translocation STAT-3.
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spelling pubmed-74991102020-09-28 Ganoderma lucidum put forth anti-tumor activity against PC-3 prostate cancer cells via inhibition of Jak-1/STAT-3 activity Wang, Xiaoming Wang, Bo Zhou, Liquan Wang, Xiang Veeraraghavan, Vishnu Priya Mohan, Surapaneni Krishna Xin, Feng Saudi J Biol Sci Original Article BACKGROUND: Prostate cancer (PCA) is a frequent cancer that mainly affects the men. Studying growth feature pathways modified during PCA development may facilitate researchers to expand embattled therapeutic strategies for prostate cancer. In present study, we examined the anticancer potentials of Ganoderma lucidum against the prostate cancer (PC-3) cells by inflection of JAK-1/STAT-3 signalling pathway. METHODS: The cytotoxicity of G. lucidum against the PC-3 cells was examined by MTT assay. The ROS production was monitored by using DCFH-DA staining. The apoptotic morphological alterations stimulatory potential of G. lucidum on PC-3 cells was inspected through the dual staining. The expression of Bcl-2, JAK-1, STAT3, Bax and CyclinD1 proteins were measured by western blotting. The caspase-3 and 9 functions were condensed by assay kit. RESULTS: Findings demonstrates the Ganoderma lucidum convince cytotoxicity, accretion of ROS, and apoptosis stimulation in PC-3 cells. In addition, signal transducer and activating transcription (STAT-3) is a successive oncogenic transcriptional factor that regularizes multiplication and apoptosis in cells. Discretion of STAT-3 transcription deliberated as original approach to hinder prostate cell growth. In present exploration, we ascertain that Ganoderma lucidum hold back STAT-3 translocation, in that way dropping the eminent expression of, BCL-2, cyclin-D1 and declined the Bax, caspase-3 and 9 expressions in PC-3 cells. CONCLUSION: In the end our finding concluded that Ganoderma lucidum hinder prostate cell development and convinces apoptosis via hampering the translocation STAT-3. Elsevier 2020-10 2020-06-03 /pmc/articles/PMC7499110/ /pubmed/32994721 http://dx.doi.org/10.1016/j.sjbs.2020.05.044 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Wang, Xiaoming
Wang, Bo
Zhou, Liquan
Wang, Xiang
Veeraraghavan, Vishnu Priya
Mohan, Surapaneni Krishna
Xin, Feng
Ganoderma lucidum put forth anti-tumor activity against PC-3 prostate cancer cells via inhibition of Jak-1/STAT-3 activity
title Ganoderma lucidum put forth anti-tumor activity against PC-3 prostate cancer cells via inhibition of Jak-1/STAT-3 activity
title_full Ganoderma lucidum put forth anti-tumor activity against PC-3 prostate cancer cells via inhibition of Jak-1/STAT-3 activity
title_fullStr Ganoderma lucidum put forth anti-tumor activity against PC-3 prostate cancer cells via inhibition of Jak-1/STAT-3 activity
title_full_unstemmed Ganoderma lucidum put forth anti-tumor activity against PC-3 prostate cancer cells via inhibition of Jak-1/STAT-3 activity
title_short Ganoderma lucidum put forth anti-tumor activity against PC-3 prostate cancer cells via inhibition of Jak-1/STAT-3 activity
title_sort ganoderma lucidum put forth anti-tumor activity against pc-3 prostate cancer cells via inhibition of jak-1/stat-3 activity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499110/
https://www.ncbi.nlm.nih.gov/pubmed/32994721
http://dx.doi.org/10.1016/j.sjbs.2020.05.044
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