Cargando…

Inhibition of ALAS1 activity exerts anti-tumour effects on colorectal cancer in vitro

BACKGROUND/AIMS: Colorectal cancer (CRC) is the third most common malignant tumour worldwide and the second leading cause of cancer-related deaths. Commonly, 5'-aminolevulinic acid synthase1 (ALAS1) is the rate-limiting enzyme for haem biosynthesis. Recent studies have shown that ALAS1 is invol...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Yalei, Zhang, Xiaoyun, Liu, Yabin, Ma, Yiping, Kong, Pong, Bai, Tianliang, Han, Mei, Li, Binghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392291/
https://www.ncbi.nlm.nih.gov/pubmed/32270771
http://dx.doi.org/10.4103/sjg.SJG_477_19
_version_ 1783564817906270208
author Zhao, Yalei
Zhang, Xiaoyun
Liu, Yabin
Ma, Yiping
Kong, Pong
Bai, Tianliang
Han, Mei
Li, Binghui
author_facet Zhao, Yalei
Zhang, Xiaoyun
Liu, Yabin
Ma, Yiping
Kong, Pong
Bai, Tianliang
Han, Mei
Li, Binghui
author_sort Zhao, Yalei
collection PubMed
description BACKGROUND/AIMS: Colorectal cancer (CRC) is the third most common malignant tumour worldwide and the second leading cause of cancer-related deaths. Commonly, 5'-aminolevulinic acid synthase1 (ALAS1) is the rate-limiting enzyme for haem biosynthesis. Recent studies have shown that ALAS1 is involved in a number of cellular functions and has significant effects on non-small cell lung cancer (NSCLC). However, current concepts of disease pathogenesis fail to fully explain the role of ALAS1 expression and biological functions in CRC. MATERIALS AND METHODS: A total of 67 paired tumour tissues and adjacent colorectal tissues were used to detect ALAS1 levels and further analyse the correlation between ALAS1 expression levels and clinical features. Using HCT116 cell lines, we studied the impact of ALAS1 on biological function by knocking down or inhibiting ALAS1. RESULTS: We found an increase in the levels of ALAS1 in cancer tissues compared to adjacent colorectal tissues. The increase in ALAS1 expression was closely related to the invasion depth, N staging and tumour size of CRC patients. The proliferation and metastasis of CRC cells could be inhibited by suppressing ALAS1. CONCLUSIONS: The abnormal expression of ALAS1 is closely related to the proliferation and metastasis of CRC cells, suggesting that ALAS1 may be a novel therapeutic target for the treatment of CRC.
format Online
Article
Text
id pubmed-7392291
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Wolters Kluwer - Medknow
record_format MEDLINE/PubMed
spelling pubmed-73922912020-08-12 Inhibition of ALAS1 activity exerts anti-tumour effects on colorectal cancer in vitro Zhao, Yalei Zhang, Xiaoyun Liu, Yabin Ma, Yiping Kong, Pong Bai, Tianliang Han, Mei Li, Binghui Saudi J Gastroenterol Original Article BACKGROUND/AIMS: Colorectal cancer (CRC) is the third most common malignant tumour worldwide and the second leading cause of cancer-related deaths. Commonly, 5'-aminolevulinic acid synthase1 (ALAS1) is the rate-limiting enzyme for haem biosynthesis. Recent studies have shown that ALAS1 is involved in a number of cellular functions and has significant effects on non-small cell lung cancer (NSCLC). However, current concepts of disease pathogenesis fail to fully explain the role of ALAS1 expression and biological functions in CRC. MATERIALS AND METHODS: A total of 67 paired tumour tissues and adjacent colorectal tissues were used to detect ALAS1 levels and further analyse the correlation between ALAS1 expression levels and clinical features. Using HCT116 cell lines, we studied the impact of ALAS1 on biological function by knocking down or inhibiting ALAS1. RESULTS: We found an increase in the levels of ALAS1 in cancer tissues compared to adjacent colorectal tissues. The increase in ALAS1 expression was closely related to the invasion depth, N staging and tumour size of CRC patients. The proliferation and metastasis of CRC cells could be inhibited by suppressing ALAS1. CONCLUSIONS: The abnormal expression of ALAS1 is closely related to the proliferation and metastasis of CRC cells, suggesting that ALAS1 may be a novel therapeutic target for the treatment of CRC. Wolters Kluwer - Medknow 2020-04-06 /pmc/articles/PMC7392291/ /pubmed/32270771 http://dx.doi.org/10.4103/sjg.SJG_477_19 Text en Copyright: © 2020 Saudi Journal of Gastroenterology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Zhao, Yalei
Zhang, Xiaoyun
Liu, Yabin
Ma, Yiping
Kong, Pong
Bai, Tianliang
Han, Mei
Li, Binghui
Inhibition of ALAS1 activity exerts anti-tumour effects on colorectal cancer in vitro
title Inhibition of ALAS1 activity exerts anti-tumour effects on colorectal cancer in vitro
title_full Inhibition of ALAS1 activity exerts anti-tumour effects on colorectal cancer in vitro
title_fullStr Inhibition of ALAS1 activity exerts anti-tumour effects on colorectal cancer in vitro
title_full_unstemmed Inhibition of ALAS1 activity exerts anti-tumour effects on colorectal cancer in vitro
title_short Inhibition of ALAS1 activity exerts anti-tumour effects on colorectal cancer in vitro
title_sort inhibition of alas1 activity exerts anti-tumour effects on colorectal cancer in vitro
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392291/
https://www.ncbi.nlm.nih.gov/pubmed/32270771
http://dx.doi.org/10.4103/sjg.SJG_477_19
work_keys_str_mv AT zhaoyalei inhibitionofalas1activityexertsantitumoureffectsoncolorectalcancerinvitro
AT zhangxiaoyun inhibitionofalas1activityexertsantitumoureffectsoncolorectalcancerinvitro
AT liuyabin inhibitionofalas1activityexertsantitumoureffectsoncolorectalcancerinvitro
AT mayiping inhibitionofalas1activityexertsantitumoureffectsoncolorectalcancerinvitro
AT kongpong inhibitionofalas1activityexertsantitumoureffectsoncolorectalcancerinvitro
AT baitianliang inhibitionofalas1activityexertsantitumoureffectsoncolorectalcancerinvitro
AT hanmei inhibitionofalas1activityexertsantitumoureffectsoncolorectalcancerinvitro
AT libinghui inhibitionofalas1activityexertsantitumoureffectsoncolorectalcancerinvitro