FOXD3 promotes the transcription of RGS13 to inhibit colorectal cancer malignant progression and CD8+ T cell apoptosis.

BACKGROUND: Regulator of G-protein signaling 13 (RGS13) plays a tumor suppressor role in a variety of cancers, but its expression, function, and regulatory mechanism in colorectal cancer (CRC) are still unclear. METHODS: , the tumor suppressive effect of RGS13 was verified by a xenograft tumor model in nude mice. Bioinformatics prediction, dual-luciferase reporter assay, and the rescue experiment were used to explore the transcriptional regulation of FOXD3 on RGS13. RESULTS: T-cell apoptosis by upregulating RGS13. CONCLUSION: T-cell apoptosis by regulating the tumor microenvironment.

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Publication Details

Journal
PubMed
Published
2026-10-30
DOI
https://doi.org/10.14670/hh-25-165
Primary Topic
Mechanisms of cancer metastasis
Type
article
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article

FOXD3 promotes the transcription of RGS13 to inhibit colorectal cancer malignant progression and CD8+ T cell apoptosis.

Xiaoqing He, Ranxing Zhang, Lei Meng, Xiaoye Fan et al.
PubMed
Mechanisms of cancer metastasis
article

FOXD3 promotes the transcription of RGS13 to inhibit colorectal cancer malignant progression and CD8+ T cell apoptosis.

Xiaoqing He, Ranxing Zhang, Lei Meng, Xiaoye Fan, Song Zheng
article en

Abstract

BACKGROUND: Regulator of G-protein signaling 13 (RGS13) plays a tumor suppressor role in a variety of cancers, but its expression, function, and regulatory mechanism in colorectal cancer (CRC) are still unclear. METHODS: , the tumor suppressive effect of RGS13 was verified by a xenograft tumor model in nude mice. Bioinformatics prediction, dual-luciferase reporter assay, and the rescue experiment were used to explore the transcriptional regulation of FOXD3 on RGS13. RESULTS: T-cell apoptosis by upregulating RGS13. CONCLUSION: T-cell apoptosis by regulating the tumor microenvironment.

PubMed
Hebei Medical University (CN), Xingtai People's Hospital (CN)
Good health and well-being
Openalex Percentile: Top 22%
Mechanisms of cancer metastasis
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