HAS-CIRCpedia-5280 sponges miR-4712-5p inhibited colon cancer autophagyinduced by human beta-defensin-1

Abstract Background Among all malignancies, colorectal cancer ranks third in incidence rate and second in mortality rate. Human beta-defensin-1 (hBD-1) has broad-spectrum antimicrobial properties, and it plays an important role in the tumor microenvironment. Circular ribonucleic acids (circRNAs) reg...

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التفاصيل البيبلوغرافية
الحاوية / القاعدة:Journal of Translational Medicine
المؤلفون الرئيسيون: Shixiang An, Jiaxian Cui, Wenhong Yang, Mingyu Zhang, Huiling Yu, Jingkun Lu, Yunpeng Tian, Lu Qiao, Xiumei Wang, Lili Bao, Pengwei Zhao
التنسيق: مقال
اللغة:الإنجليزية
منشور في: BMC 2025-03-01
الموضوعات:
الوصول للمادة أونلاين:https://doi.org/10.1186/s12967-024-05860-x
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author Shixiang An
Jiaxian Cui
Wenhong Yang
Mingyu Zhang
Huiling Yu
Jingkun Lu
Yunpeng Tian
Lu Qiao
Xiumei Wang
Lili Bao
Pengwei Zhao
author_facet Shixiang An
Jiaxian Cui
Wenhong Yang
Mingyu Zhang
Huiling Yu
Jingkun Lu
Yunpeng Tian
Lu Qiao
Xiumei Wang
Lili Bao
Pengwei Zhao
author_sort Shixiang An
collection DOAJ
container_title Journal of Translational Medicine
description Abstract Background Among all malignancies, colorectal cancer ranks third in incidence rate and second in mortality rate. Human beta-defensin-1 (hBD-1) has broad-spectrum antimicrobial properties, and it plays an important role in the tumor microenvironment. Circular ribonucleic acids (circRNAs) regulate the proliferation and progression of colorectal cancer cells via cancer-related signaling pathways. Methods Cell proliferation was assessed using the Cell Counting Kit-8 assay to determine the optimal hBD-1 concentration. Intracellular autophagic vesicles were visualized via monodansylcadaverine staining. In addition, the levels of AKT and mammalian target of rapamycin (mTOR)-associated signaling proteins were analyzed via Western blot analysis. CircRNA microarrays and quantitative real-time polymerase chain reaction were used to identify differentially expressed circRNAs in colon cancer cell lines. The functional role of HAS-CIRCpedia-5280 in vitro was demonstrated by overexpressing HAS-CIRCpedia-5280 and inhibiting miR-4712-5p. HAS-CIRCpedia-5280 could be a sponge of miR-4712-5p, mimicking the effect induced by HAS-CIRCpedia-5280 overexpression in colon cancer cells. Results hBD-1 inhibited the proliferation of colon cancer cells and increased the number of intracellular autophagic vesicles. In addition, hBD-1 inhibited the AKT/mTOR signaling pathway, thereby enhancing cellular autophagy. Further, the interaction of HAS-CIRCpedia-5280 and miR-4712-5p was investigated. hBD-1 upregulated the expression level of HAS-CIRCpedia-5280 and downregulated the expression level of miR-4712-5p in colon cancer cells. Subsequently, the overexpression of HAS-CIRCpedia-5280 or the inhibition of miR-4712-5p activated the AKT/mTOR signaling pathway, leading to cellular autophagy inhibition. Conversely, the mimicry of miR-4712-p counteracted the effect of HAS-CIRCpedia 5280 overexpression in colon cancer cells by inhibiting the activation of the AKT/mTOR signaling pathway and, thereby, enhancing cellular autophagy. Conclusion hBD-1 can have an inhibitory effect against cell proliferation in colon cancer SW-620/HCT-116 cells via the HAS-CIRCpedia-5280/miR-4712-5p-mediated activation of autophagy.
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spelling doaj-art-e6af96c657e74789a1046b3cd9df80ca2025-08-20T01:40:18ZengBMCJournal of Translational Medicine1479-58762025-03-0123111210.1186/s12967-024-05860-xHAS-CIRCpedia-5280 sponges miR-4712-5p inhibited colon cancer autophagyinduced by human beta-defensin-1Shixiang An0Jiaxian Cui1Wenhong Yang2Mingyu Zhang3Huiling Yu4Jingkun Lu5Yunpeng Tian6Lu Qiao7Xiumei Wang8Lili Bao9Pengwei Zhao10Laboratory of Microbiology and Immunology, School of Basic Medical Science, Inner Mongolia Medical UniversityLaboratory of Microbiology and Immunology, School of Basic Medical Science, Inner Mongolia Medical UniversityLaboratory of Microbiology and Immunology, School of Basic Medical Science, Inner Mongolia Medical UniversityLaboratory of Microbiology and Immunology, School of Basic Medical Science, Inner Mongolia Medical UniversityLaboratory of Microbiology and Immunology, School of Basic Medical Science, Inner Mongolia Medical UniversityLaboratory of Microbiology and Immunology, School of Basic Medical Science, Inner Mongolia Medical UniversityLaboratory of Microbiology and Immunology, School of Basic Medical Science, Inner Mongolia Medical UniversityLaboratory of Microbiology and Immunology, School of Basic Medical Science, Inner Mongolia Medical UniversityMedical Oncology, Affiliated People’s Hospital of Inner Mongolia Medical UniversityLaboratory of Microbiology and Immunology, School of Basic Medical Science, Inner Mongolia Medical UniversityLaboratory of Microbiology and Immunology, School of Basic Medical Science, Inner Mongolia Medical UniversityAbstract Background Among all malignancies, colorectal cancer ranks third in incidence rate and second in mortality rate. Human beta-defensin-1 (hBD-1) has broad-spectrum antimicrobial properties, and it plays an important role in the tumor microenvironment. Circular ribonucleic acids (circRNAs) regulate the proliferation and progression of colorectal cancer cells via cancer-related signaling pathways. Methods Cell proliferation was assessed using the Cell Counting Kit-8 assay to determine the optimal hBD-1 concentration. Intracellular autophagic vesicles were visualized via monodansylcadaverine staining. In addition, the levels of AKT and mammalian target of rapamycin (mTOR)-associated signaling proteins were analyzed via Western blot analysis. CircRNA microarrays and quantitative real-time polymerase chain reaction were used to identify differentially expressed circRNAs in colon cancer cell lines. The functional role of HAS-CIRCpedia-5280 in vitro was demonstrated by overexpressing HAS-CIRCpedia-5280 and inhibiting miR-4712-5p. HAS-CIRCpedia-5280 could be a sponge of miR-4712-5p, mimicking the effect induced by HAS-CIRCpedia-5280 overexpression in colon cancer cells. Results hBD-1 inhibited the proliferation of colon cancer cells and increased the number of intracellular autophagic vesicles. In addition, hBD-1 inhibited the AKT/mTOR signaling pathway, thereby enhancing cellular autophagy. Further, the interaction of HAS-CIRCpedia-5280 and miR-4712-5p was investigated. hBD-1 upregulated the expression level of HAS-CIRCpedia-5280 and downregulated the expression level of miR-4712-5p in colon cancer cells. Subsequently, the overexpression of HAS-CIRCpedia-5280 or the inhibition of miR-4712-5p activated the AKT/mTOR signaling pathway, leading to cellular autophagy inhibition. Conversely, the mimicry of miR-4712-p counteracted the effect of HAS-CIRCpedia 5280 overexpression in colon cancer cells by inhibiting the activation of the AKT/mTOR signaling pathway and, thereby, enhancing cellular autophagy. Conclusion hBD-1 can have an inhibitory effect against cell proliferation in colon cancer SW-620/HCT-116 cells via the HAS-CIRCpedia-5280/miR-4712-5p-mediated activation of autophagy.https://doi.org/10.1186/s12967-024-05860-xColon cancerHuman β-defensin-1Circular RNAsmiRNA spongeAutophagy
spellingShingle Shixiang An
Jiaxian Cui
Wenhong Yang
Mingyu Zhang
Huiling Yu
Jingkun Lu
Yunpeng Tian
Lu Qiao
Xiumei Wang
Lili Bao
Pengwei Zhao
HAS-CIRCpedia-5280 sponges miR-4712-5p inhibited colon cancer autophagyinduced by human beta-defensin-1
Colon cancer
Human β-defensin-1
Circular RNAs
miRNA sponge
Autophagy
title HAS-CIRCpedia-5280 sponges miR-4712-5p inhibited colon cancer autophagyinduced by human beta-defensin-1
title_full HAS-CIRCpedia-5280 sponges miR-4712-5p inhibited colon cancer autophagyinduced by human beta-defensin-1
title_fullStr HAS-CIRCpedia-5280 sponges miR-4712-5p inhibited colon cancer autophagyinduced by human beta-defensin-1
title_full_unstemmed HAS-CIRCpedia-5280 sponges miR-4712-5p inhibited colon cancer autophagyinduced by human beta-defensin-1
title_short HAS-CIRCpedia-5280 sponges miR-4712-5p inhibited colon cancer autophagyinduced by human beta-defensin-1
title_sort has circpedia 5280 sponges mir 4712 5p inhibited colon cancer autophagyinduced by human beta defensin 1
topic Colon cancer
Human β-defensin-1
Circular RNAs
miRNA sponge
Autophagy
url https://doi.org/10.1186/s12967-024-05860-x
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