GnRHR inhibits the malignant progression of triple-negative breast cancer by upregulating FOS and IFI44L

Gonadotropin-releasing hormone receptor (GnRHR) has been identified as a factor that hinders the malignant advancement of triple-negative breast cancer (TNBC). Nevertheless, the specific molecular mechanism responsible for this impact remains unclear. This study demonstrates that GnRHR exhibits low expression levels in TNBC, which correlates with an unfavorable prognosis for patients. GnRHR promotes the expression of FOS, subsequently enhancing IFI44L transcription and expression, thereby inhibiting TNBC cell proliferation, migration, and invasion. Goserelin reduced the growth rate of TNBC tumors in nude mice, resulting in elevated levels of GnRHR, FOS, and IFI44L in tumor tissues, while the expression of Ki67, vimentin, and N-cadherin decreased. Overall, our results reveal that GnRHR suppresses the malignant progression of TNBC by upregulating FOS and IFI44L. Goserelin slows down the proliferation of TNBC tumors in vivo through the GnRHR/FOS/IFI44L pathway, which may present a new therapeutic approach for the management of TNBC.

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Publication Details

Journal
Genomics
Published
2025-02-23
DOI
https://doi.org/10.1016/j.ygeno.2025.111021
Citations
1
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
0.94
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article

GnRHR inhibits the malignant progression of triple-negative breast cancer by upregulating FOS and IFI44L

Wanxin Wu, Chao Han, Ning Lü, Xue Li et al.
1 citations
Genomics
Cancer-related molecular mechanisms research
0.94
article

GnRHR inhibits the malignant progression of triple-negative breast cancer by upregulating FOS and IFI44L

Wanxin Wu, Chao Han, Ning Lü, Xue Li, Xiang Lü, Caiping Chen
article en
1 citations

Abstract

Gonadotropin-releasing hormone receptor (GnRHR) has been identified as a factor that hinders the malignant advancement of triple-negative breast cancer (TNBC). Nevertheless, the specific molecular mechanism responsible for this impact remains unclear. This study demonstrates that GnRHR exhibits low expression levels in TNBC, which correlates with an unfavorable prognosis for patients. GnRHR promotes the expression of FOS, subsequently enhancing IFI44L transcription and expression, thereby inhibiting TNBC cell proliferation, migration, and invasion. Goserelin reduced the growth rate of TNBC tumors in nude mice, resulting in elevated levels of GnRHR, FOS, and IFI44L in tumor tissues, while the expression of Ki67, vimentin, and N-cadherin decreased. Overall, our results reveal that GnRHR suppresses the malignant progression of TNBC by upregulating FOS and IFI44L. Goserelin slows down the proliferation of TNBC tumors in vivo through the GnRHR/FOS/IFI44L pathway, which may present a new therapeutic approach for the management of TNBC.

GenomicsVol. 117(2)
Jiaxing University (CN), First Hospital of Jiaxing (CN)
Good health and well-being
Openalex Percentile: Top 28%
Cancer-related molecular mechanisms research
0.94
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