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DOI 10.1038/s41598-024-79688-2

Медицинская библиотека · Scientific reports · 2024

LATS2 and FAT4 as key candidate genes of hippo pathway associated with the risk and progression of breast cancer: an in-silico approach.

Sadaf, Zafar Mubashir, Massey Sheersh, Aloliqi Abdulaziz A, Anwar Sadaf, Ali Abrar, Hussain Malik Asif, Bhardwaj Tulika, Dev Kapil

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Аннотация

BACKGROUND

The 2020 cancer report states that breast cancer remains a significant cause of death for females, despite the use of various strategies for early detection and treatment. However, there are still gaps in the fight against this disease. Researchers are exploring the hippo pathway, one of eight significant pathways involved in cancer progression, for potential biomarkers to use in personalized therapeutics.

METHODS

The current study used bioinformatic tools such as DEGs analysis, Methsurv, Km Plotter to generate data that can predict molecular biomarkers associated with hippo pathway in breast cancer development and treatment. The protein-protein interaction pathway was generated using the STRING database to find associations of hippo pathway genes with other dysregulated genes in breast cancer datasets. A disease enrichment study was also done to explore the potential of the hippo pathway in various aspects.

RESULTS

LATS2 and FAT4 genes of the hippo pathway have shown an interesting association with overall survival, hypermethylation, genetic alterations, and decreased expression levels in the breast cancer cohort. Our findings suggest that both of these genes are associated with breast cancer progression and diagnosis and can be utilized as predictive biomarkers by oncologists for personalized therapy in patients.

Для цитирования: Sadaf, Zafar Mubashir, Massey Sheersh, Aloliqi Abdulaziz A, Anwar Sadaf, Ali Abrar, Hussain Malik Asif, Bhardwaj Tulika, Dev Kapil. LATS2 and FAT4 as key candidate genes of hippo pathway associated with the risk and progression of breast cancer: an in-silico approach.. Scientific reports. 2024. DOI: 10.1038/s41598-024-79688-2.

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