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LEP as a potential biomarker in prognosis of breast cancer

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Abstract Purpose Obesity strongly affects the prognosis of various malignancies, including breast cancer. Leptin (LEP) may be associated with obesity and breast cancer prognosis. The purpose of our study was to determine the prognostic value of LEP in breast cancer. Method We conducted a multi-omic analysis to determine the prognostic role of LEP. Different public bioinformatics platforms (Oncomine, Gene Expression Profiling Interactive Analysis, University of California Santa Cruz Xena, bc-GenExMiner, PrognoScan database, R2-Kaplan–Meier Scanner, UALCAN, Search Tool for the Retrieval of Interacting Genes/Proteins database , and The Database for Annotation, Visualization and Integrated Discovery) were used to evaluate the roles of LEP. Clinicopathological variables were evaluated. Results LEP was downregulated in breast cancer tissues compared to levels in normal tissues. By co-expressed gene analysis, a positive correlation between LEP and SLC19A3 was observed. Based on the clinicopathological analysis, low LEP expression was associated with older age, higher stage, lymph node status, human epidermal growth factor receptor 2 (HER2) status, estrogen receptor (ER+) positivity, and progesterone receptor (PR+) positivity. Kaplan–Meier survival analysis showed that low LEP expression indicated a poorer prognosis. LEP is hypermethylated in breast cancer tissues in PrognoScan and R2-Kaplan Meier Scanner, and low LEP expression was correlated with poor prognosis. LEP protein–protein interactions were analyzed using Search Tool for the Retrieval of Interacting Genes/Proteins database. Gene ontology analysis results showed that cellular component is mainly associated with the endosome lumen, cytosol, and secretory granules and is upregulated. For the biological process energy reserve, metabolic processes exhibited the greatest regulation compared to the others. In molecular function, it was mainly enriched in a variety of combinations, but hormone activity showed the highest regulation. Conclusion Our study provides evidence for the prognostic role of LEP in breast cancer and as a novel potential therapeutic target in such malignancies. Nevertheless, further validation is required.
Title: LEP as a potential biomarker in prognosis of breast cancer
Description:
Abstract Purpose Obesity strongly affects the prognosis of various malignancies, including breast cancer.
Leptin (LEP) may be associated with obesity and breast cancer prognosis.
The purpose of our study was to determine the prognostic value of LEP in breast cancer.
Method We conducted a multi-omic analysis to determine the prognostic role of LEP.
Different public bioinformatics platforms (Oncomine, Gene Expression Profiling Interactive Analysis, University of California Santa Cruz Xena, bc-GenExMiner, PrognoScan database, R2-Kaplan–Meier Scanner, UALCAN, Search Tool for the Retrieval of Interacting Genes/Proteins database , and The Database for Annotation, Visualization and Integrated Discovery) were used to evaluate the roles of LEP.
Clinicopathological variables were evaluated.
Results LEP was downregulated in breast cancer tissues compared to levels in normal tissues.
By co-expressed gene analysis, a positive correlation between LEP and SLC19A3 was observed.
Based on the clinicopathological analysis, low LEP expression was associated with older age, higher stage, lymph node status, human epidermal growth factor receptor 2 (HER2) status, estrogen receptor (ER+) positivity, and progesterone receptor (PR+) positivity.
Kaplan–Meier survival analysis showed that low LEP expression indicated a poorer prognosis.
LEP is hypermethylated in breast cancer tissues in PrognoScan and R2-Kaplan Meier Scanner, and low LEP expression was correlated with poor prognosis.
LEP protein–protein interactions were analyzed using Search Tool for the Retrieval of Interacting Genes/Proteins database.
Gene ontology analysis results showed that cellular component is mainly associated with the endosome lumen, cytosol, and secretory granules and is upregulated.
For the biological process energy reserve, metabolic processes exhibited the greatest regulation compared to the others.
In molecular function, it was mainly enriched in a variety of combinations, but hormone activity showed the highest regulation.
Conclusion Our study provides evidence for the prognostic role of LEP in breast cancer and as a novel potential therapeutic target in such malignancies.
Nevertheless, further validation is required.

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