circNHSL1 inhibits proliferation and promotes apoptosis of human breast cancer cell line through regulating miR-125b-5p/HMGB3 axis

Objective To investigate the regulation of miR-125b-5p/HMGB3 axis by circNHSL1 on the biological behavior of breast cancer cells. Methods The breast cancer cells T47D were divided into si-NC group, si-circNHSL1 group, miR-NC group, and miR-125b-5p mimic group and si-circNHSL1+miR-125b-5p inhibitor...

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Main Author: LI Huan, XIE Xianxin
Format: Article
Language:zho
Published: Institute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College. 2024-12-01
Series:Jichu yixue yu linchuang
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Online Access:https://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2024-44-12-1678.pdf
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author LI Huan, XIE Xianxin
author_facet LI Huan, XIE Xianxin
author_sort LI Huan, XIE Xianxin
collection DOAJ
description Objective To investigate the regulation of miR-125b-5p/HMGB3 axis by circNHSL1 on the biological behavior of breast cancer cells. Methods The breast cancer cells T47D were divided into si-NC group, si-circNHSL1 group, miR-NC group, and miR-125b-5p mimic group and si-circNHSL1+miR-125b-5p inhibitor group. The expression of circNHSL1 and miR-125b-5p in breast cancer tissues and adjacent tissues was determined using RT-qPCR. Western blot was conducted to detect the protein expression of high mobility group protein 3 (HMGB3). Dual luciferase reporter gene assay was used to confirm the interaction between circNHSL1 and miR-125b-5p, miR-125b-5p and HMGB3. The proliferation rate was measured by CCK-8 method; the colony formation assay was applied to detect the colony formation numbers; flow cytometry was used to measure cell apoptosis rate; Transwell assay was used to detect the numbers of migratory and invasive cells. Results Compared with adjacent tissues, circNHSL1 and HMGB3 expression in breast cancer tissues was significantly increased (P<0.05), while the expression of miR-125b-5p was significantly decreased (P<0.05). miR-125b-5p directly bound to circNHSL1 and HMGB3, respectively. The circNHSL1 knockdown down regulated circNHSL1 and HMGB3 expression and upregulated miR-125b-5p expression in T47D cells (P<0.05). After transfection with miR-125b-5p mimic, miR-125b-5p expression was up-regulated and HMGB3 expression was down-regulated (P<0.05). Moreover, transfection of miR-125b-5p inhibitor reversed the effect of circNHSL1 silencing on the expression of miR-125b-5p and HMGB3. Low expression of circNHSL1 or high expression of miR-125b-5p increased the cell inhibition rate, colony formation and apoptosis rate of T47D and decreased the number of migratory and invasive cells (P<0.05). Moreover, transfection of miR-125b-5p inhibitor saved the effect of circNHSL1 silencing on cell phenotypes (P<0.05). Conclusions Interfering with circNHSL1 might promote cell apoptosis and inhibit cell proliferation, migration and invasion in breast cancer cell by up-regulating the miR-125b-5p/HMGB3 axis.
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issn 1001-6325
language zho
publishDate 2024-12-01
publisher Institute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College.
record_format Article
series Jichu yixue yu linchuang
spelling doaj-art-94736fb4bd4a488ab61be7a1a20bfaf42025-08-20T02:50:23ZzhoInstitute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College.Jichu yixue yu linchuang1001-63252024-12-0144121678168410.16352/j.issn.1001-6325.2024.12.1678circNHSL1 inhibits proliferation and promotes apoptosis of human breast cancer cell line through regulating miR-125b-5p/HMGB3 axisLI Huan, XIE Xianxin0Department of Breast Medicine, Liaoning Cancer Hospital,Shenyang 110042, ChinaObjective To investigate the regulation of miR-125b-5p/HMGB3 axis by circNHSL1 on the biological behavior of breast cancer cells. Methods The breast cancer cells T47D were divided into si-NC group, si-circNHSL1 group, miR-NC group, and miR-125b-5p mimic group and si-circNHSL1+miR-125b-5p inhibitor group. The expression of circNHSL1 and miR-125b-5p in breast cancer tissues and adjacent tissues was determined using RT-qPCR. Western blot was conducted to detect the protein expression of high mobility group protein 3 (HMGB3). Dual luciferase reporter gene assay was used to confirm the interaction between circNHSL1 and miR-125b-5p, miR-125b-5p and HMGB3. The proliferation rate was measured by CCK-8 method; the colony formation assay was applied to detect the colony formation numbers; flow cytometry was used to measure cell apoptosis rate; Transwell assay was used to detect the numbers of migratory and invasive cells. Results Compared with adjacent tissues, circNHSL1 and HMGB3 expression in breast cancer tissues was significantly increased (P<0.05), while the expression of miR-125b-5p was significantly decreased (P<0.05). miR-125b-5p directly bound to circNHSL1 and HMGB3, respectively. The circNHSL1 knockdown down regulated circNHSL1 and HMGB3 expression and upregulated miR-125b-5p expression in T47D cells (P<0.05). After transfection with miR-125b-5p mimic, miR-125b-5p expression was up-regulated and HMGB3 expression was down-regulated (P<0.05). Moreover, transfection of miR-125b-5p inhibitor reversed the effect of circNHSL1 silencing on the expression of miR-125b-5p and HMGB3. Low expression of circNHSL1 or high expression of miR-125b-5p increased the cell inhibition rate, colony formation and apoptosis rate of T47D and decreased the number of migratory and invasive cells (P<0.05). Moreover, transfection of miR-125b-5p inhibitor saved the effect of circNHSL1 silencing on cell phenotypes (P<0.05). Conclusions Interfering with circNHSL1 might promote cell apoptosis and inhibit cell proliferation, migration and invasion in breast cancer cell by up-regulating the miR-125b-5p/HMGB3 axis.https://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2024-44-12-1678.pdfbreast cancer|circnhsl1|mir-125b-5p|high mobility group protein 3(hmgb3)
spellingShingle LI Huan, XIE Xianxin
circNHSL1 inhibits proliferation and promotes apoptosis of human breast cancer cell line through regulating miR-125b-5p/HMGB3 axis
Jichu yixue yu linchuang
breast cancer|circnhsl1|mir-125b-5p|high mobility group protein 3(hmgb3)
title circNHSL1 inhibits proliferation and promotes apoptosis of human breast cancer cell line through regulating miR-125b-5p/HMGB3 axis
title_full circNHSL1 inhibits proliferation and promotes apoptosis of human breast cancer cell line through regulating miR-125b-5p/HMGB3 axis
title_fullStr circNHSL1 inhibits proliferation and promotes apoptosis of human breast cancer cell line through regulating miR-125b-5p/HMGB3 axis
title_full_unstemmed circNHSL1 inhibits proliferation and promotes apoptosis of human breast cancer cell line through regulating miR-125b-5p/HMGB3 axis
title_short circNHSL1 inhibits proliferation and promotes apoptosis of human breast cancer cell line through regulating miR-125b-5p/HMGB3 axis
title_sort circnhsl1 inhibits proliferation and promotes apoptosis of human breast cancer cell line through regulating mir 125b 5p hmgb3 axis
topic breast cancer|circnhsl1|mir-125b-5p|high mobility group protein 3(hmgb3)
url https://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2024-44-12-1678.pdf
work_keys_str_mv AT lihuanxiexianxin circnhsl1inhibitsproliferationandpromotesapoptosisofhumanbreastcancercelllinethroughregulatingmir125b5phmgb3axis