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Sanjie Yiliu Formula Inhibits Colorectal Cancer Growth by Suppression of Proliferation and Induction of Apoptosis
[Image: see text] Colorectal cancer (CRC) is one of the most common malignancies worldwide. As current therapies toward CRC, including chemotherapy and radiotherapy, pose limitations, such as multidrug resistance (MDR) as well as the intrinsic and potential cytotoxic effects, necessitating to find m...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992181/ https://www.ncbi.nlm.nih.gov/pubmed/33778287 http://dx.doi.org/10.1021/acsomega.0c05565 |
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author | Tang, Rong Zhu Li, Zhang Zhi Hu, Dan Kanwal, Fariha Yuan, Cheng Bin Mustaqeem, Muhammad Batool, Aima Iram Rehman, Muhammad Fayyaz ur |
author_facet | Tang, Rong Zhu Li, Zhang Zhi Hu, Dan Kanwal, Fariha Yuan, Cheng Bin Mustaqeem, Muhammad Batool, Aima Iram Rehman, Muhammad Fayyaz ur |
author_sort | Tang, Rong Zhu |
collection | PubMed |
description | [Image: see text] Colorectal cancer (CRC) is one of the most common malignancies worldwide. As current therapies toward CRC, including chemotherapy and radiotherapy, pose limitations, such as multidrug resistance (MDR) as well as the intrinsic and potential cytotoxic effects, necessitating to find more effective treatment options with fewer side effects, traditional Chinese medicine (TCM) has an advantage in complementary therapies. In the present study, 3-(4,5-dimethylthiozol-2-yl)-2,5-diphenyltetrazolium bromide (MTT assays), trypan blue staining, colony formation, 4,6-diamidino-2-phenylindole dihydrochloride (DAPI) staining, cell cycle determination, and Annexin V-FITC/PI staining were used to examine the efficacy of Sanjie Yiliu Formula (SJYLF) against CRC proliferation and to investigate its underlying molecular mechanisms through protein expression of various proapoptotic factors by quantitative polymerase chain reaction (q-PCR) and Western blotting. This four-herb-TCM SJYLF can be suggested as one of the decoctions clinically effective in late-stage cancer treatment. Our results suggest that SJYLF robustly decreased the viability of only CRC cell lines (HCT-8, SW-480, HT-29, and DLD-1) and not the normal human kidney cells (HK-2). Moreover, SJYLF significantly suppressed proliferation and induced apoptosis in HCT-8 and downregulated cyclin D1, CDK4, and BCL-2, while Bax expression was upregulated at both mRNA and protein expression levels. |
format | Online Article Text |
id | pubmed-7992181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79921812021-03-26 Sanjie Yiliu Formula Inhibits Colorectal Cancer Growth by Suppression of Proliferation and Induction of Apoptosis Tang, Rong Zhu Li, Zhang Zhi Hu, Dan Kanwal, Fariha Yuan, Cheng Bin Mustaqeem, Muhammad Batool, Aima Iram Rehman, Muhammad Fayyaz ur ACS Omega [Image: see text] Colorectal cancer (CRC) is one of the most common malignancies worldwide. As current therapies toward CRC, including chemotherapy and radiotherapy, pose limitations, such as multidrug resistance (MDR) as well as the intrinsic and potential cytotoxic effects, necessitating to find more effective treatment options with fewer side effects, traditional Chinese medicine (TCM) has an advantage in complementary therapies. In the present study, 3-(4,5-dimethylthiozol-2-yl)-2,5-diphenyltetrazolium bromide (MTT assays), trypan blue staining, colony formation, 4,6-diamidino-2-phenylindole dihydrochloride (DAPI) staining, cell cycle determination, and Annexin V-FITC/PI staining were used to examine the efficacy of Sanjie Yiliu Formula (SJYLF) against CRC proliferation and to investigate its underlying molecular mechanisms through protein expression of various proapoptotic factors by quantitative polymerase chain reaction (q-PCR) and Western blotting. This four-herb-TCM SJYLF can be suggested as one of the decoctions clinically effective in late-stage cancer treatment. Our results suggest that SJYLF robustly decreased the viability of only CRC cell lines (HCT-8, SW-480, HT-29, and DLD-1) and not the normal human kidney cells (HK-2). Moreover, SJYLF significantly suppressed proliferation and induced apoptosis in HCT-8 and downregulated cyclin D1, CDK4, and BCL-2, while Bax expression was upregulated at both mRNA and protein expression levels. American Chemical Society 2021-03-09 /pmc/articles/PMC7992181/ /pubmed/33778287 http://dx.doi.org/10.1021/acsomega.0c05565 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Tang, Rong Zhu Li, Zhang Zhi Hu, Dan Kanwal, Fariha Yuan, Cheng Bin Mustaqeem, Muhammad Batool, Aima Iram Rehman, Muhammad Fayyaz ur Sanjie Yiliu Formula Inhibits Colorectal Cancer Growth by Suppression of Proliferation and Induction of Apoptosis |
title | Sanjie Yiliu Formula Inhibits Colorectal Cancer Growth
by Suppression of Proliferation and Induction of Apoptosis |
title_full | Sanjie Yiliu Formula Inhibits Colorectal Cancer Growth
by Suppression of Proliferation and Induction of Apoptosis |
title_fullStr | Sanjie Yiliu Formula Inhibits Colorectal Cancer Growth
by Suppression of Proliferation and Induction of Apoptosis |
title_full_unstemmed | Sanjie Yiliu Formula Inhibits Colorectal Cancer Growth
by Suppression of Proliferation and Induction of Apoptosis |
title_short | Sanjie Yiliu Formula Inhibits Colorectal Cancer Growth
by Suppression of Proliferation and Induction of Apoptosis |
title_sort | sanjie yiliu formula inhibits colorectal cancer growth
by suppression of proliferation and induction of apoptosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992181/ https://www.ncbi.nlm.nih.gov/pubmed/33778287 http://dx.doi.org/10.1021/acsomega.0c05565 |
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