KAISO Promotes Poor Prognosis in Hepatocellular Carcinoma Patients by Enhancing Neutrophil Infiltration via IGFBP1 DOI

Zhou Jiang,

Yiqiang Pang,

Haojun Wang

и другие.

Research Square (Research Square), Год журнала: 2024, Номер unknown

Опубликована: Сен. 18, 2024

Abstract Background KAISO is a transcriptional regulator involved in gene expression, cell proliferation, and apoptosis, linked to cancer prognosis tumor aggressiveness, making it potential bi-omarker therapeutic target. Methods: We used bioinformatics analyses evaluate expression its effect on survival across 33 types of pan-cancer. also examined the link between immune infiltration. To investigate control down-stream proteins by KAISO, we dual-luciferase reporter assays, electrophoretic mobility shift assays (EMSA), chromatin immunoprecipitation (ChIP). Additionally, validated role regulating infiltration using subcutaneous model animals human samples. Results: Our research revealed that crucial growth progression various malignancies, including hepatocellular carcinoma (HCC). demonstrated high associated with poor HCC. was found regulate transcription IGFBP1 neutrophil influence HCC pro-liferation through cycle-related molecular pathways. Finally, confirmed reducing can inhibit growth. Conclusion: findings suggest could be an important biomarker target for patients.

Язык: Английский

KAISO Promotes Poor Prognosis in Hepatocellular Carcinoma Patients by Enhancing Neutrophil Infiltration via IGFBP1 DOI

Zhou Jiang,

Yiqiang Pang,

Haojun Wang

и другие.

Research Square (Research Square), Год журнала: 2024, Номер unknown

Опубликована: Сен. 18, 2024

Abstract Background KAISO is a transcriptional regulator involved in gene expression, cell proliferation, and apoptosis, linked to cancer prognosis tumor aggressiveness, making it potential bi-omarker therapeutic target. Methods: We used bioinformatics analyses evaluate expression its effect on survival across 33 types of pan-cancer. also examined the link between immune infiltration. To investigate control down-stream proteins by KAISO, we dual-luciferase reporter assays, electrophoretic mobility shift assays (EMSA), chromatin immunoprecipitation (ChIP). Additionally, validated role regulating infiltration using subcutaneous model animals human samples. Results: Our research revealed that crucial growth progression various malignancies, including hepatocellular carcinoma (HCC). demonstrated high associated with poor HCC. was found regulate transcription IGFBP1 neutrophil influence HCC pro-liferation through cycle-related molecular pathways. Finally, confirmed reducing can inhibit growth. Conclusion: findings suggest could be an important biomarker target for patients.

Язык: Английский

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