TY - JOUR
T1 - Prognostic and genomic analysis of proteasome 20s subunit alpha (PSMA) family members in breast cancer
AU - Chiao, Chung Chieh
AU - Liu, Yen Hsi
AU - Phan, Nam Nhut
AU - Ton, Nu Thuy An
AU - Ta, Hoang Dang Khoa
AU - Anuraga, Gangga
AU - Xuan, Do Thi Minh
AU - Fitriani, Fenny
AU - Hermanto, Elvira Mustikawati Putri
AU - Athoillah, Muhammad
AU - Andriani, Vivin
AU - Ajiningrum, Purity Sabila
AU - Wu, Yung Fu
AU - Lee, Kuen Haur
AU - Chuang, Jian Ying
AU - Wang, Chih Yang
AU - Kao, Tzu Jen
N1 - Funding Information:
The study was supported by grants from the Ministry of Science and Technology (MOST) of Taiwan (MOST 110-2320-B-038-017-MY3 to T.J.K., MOST 109-2320-B-038-009-MY2 to C.Y.W., and MOST 110-2636-B-038-004 to J.Y.C.) and from the Ministry of Health and Welfare Surcharge of Education Tobacco Products of Taiwan (Wan-Fang Hospital, Chi-Mei Medical Center, and Hualien Tzu-Chi Hospital Joint Cancer Center Grant?Focus on Colon Cancer Research; DP2-109-21121-03-C-03-03 and MOHW 110-TDU-B-212-144020 awarded to K.H.L.), as well as the ?TMU Research Center of Cancer Translational Medicine? from the Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education (MOE) in Taiwan.
Funding Information:
Funding: The study was supported by grants from the Ministry of Science and Technology (MOST) of Taiwan (MOST 110-2320-B-038-017-MY3 to T.J.K., MOST109-2320-B-038-009-MY2 to C.Y.W., and MOST 110-2636-B-038-004 to J.Y.C.) and from the Ministry of Health and Welfare Surcharge of Education Tobacco Products of Taiwan (Wan-Fang Hospital, Chi-Mei Medical Center, and Hualien Tzu-Chi Hospital Joint Cancer Center Grant—Focus on Colon Cancer Research; DP2-109-21121-03-C-03-03 and MOHW110-TDU-B-212-144020 awarded to K.H.L.), as well as the “TMU Research Center of Cancer Translational Medicine” from the Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education (MOE) in Taiwan.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/12
Y1 - 2021/12
N2 - The complexity of breast cancer includes many interacting biological processes, and proteasome alpha (PSMA) subunits are reported to be involved in many cancerous diseases, although the transcriptomic expression of this gene family in breast cancer still needs to be more thoroughly investigated. Consequently, we used a holistic bioinformatics approach to study the PSMA genes involved in breast cancer by integrating several well-established high-throughput databases and tools, such as cBioPortal, Oncomine, and the Kaplan–Meier plotter. Additionally, correlations of breast cancer patient survival and PSMA messenger RNA expressions were also studied. The results demonstrated that breast cancer tissues had higher expression levels of PSMA genes compared to normal breast tissues. Furthermore, PSMA2, PSMA3, PSMA4, PSMA6, and PSMA7 showed high expression levels, which were correlated with poor survival of breast cancer patients. In contrast, PSMA5 and PSMA8 had high expression levels, which were associated with good prognoses. We also found that PSMA family genes were positively correlated with the cell cycle, ubiquinone metabolism, oxidative stress, and immune response signaling, including antigen presentation by major histocom-patibility class, interferon-gamma, and the cluster of differentiation signaling. Collectively, these findings suggest that PSMA genes have the potential to serve as novel biomarkers and therapeutic targets for breast cancer. Nevertheless, the bioinformatic results from the present study would be strengthened with experimental validation in the future by prospective studies on the underlying biological mechanisms of PSMA genes and breast cancer.
AB - The complexity of breast cancer includes many interacting biological processes, and proteasome alpha (PSMA) subunits are reported to be involved in many cancerous diseases, although the transcriptomic expression of this gene family in breast cancer still needs to be more thoroughly investigated. Consequently, we used a holistic bioinformatics approach to study the PSMA genes involved in breast cancer by integrating several well-established high-throughput databases and tools, such as cBioPortal, Oncomine, and the Kaplan–Meier plotter. Additionally, correlations of breast cancer patient survival and PSMA messenger RNA expressions were also studied. The results demonstrated that breast cancer tissues had higher expression levels of PSMA genes compared to normal breast tissues. Furthermore, PSMA2, PSMA3, PSMA4, PSMA6, and PSMA7 showed high expression levels, which were correlated with poor survival of breast cancer patients. In contrast, PSMA5 and PSMA8 had high expression levels, which were associated with good prognoses. We also found that PSMA family genes were positively correlated with the cell cycle, ubiquinone metabolism, oxidative stress, and immune response signaling, including antigen presentation by major histocom-patibility class, interferon-gamma, and the cluster of differentiation signaling. Collectively, these findings suggest that PSMA genes have the potential to serve as novel biomarkers and therapeutic targets for breast cancer. Nevertheless, the bioinformatic results from the present study would be strengthened with experimental validation in the future by prospective studies on the underlying biological mechanisms of PSMA genes and breast cancer.
KW - Bioinformatics
KW - Breast cancer
KW - PSMA family genes
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U2 - 10.3390/diagnostics11122220
DO - 10.3390/diagnostics11122220
M3 - Article
AN - SCOPUS:85120303361
SN - 2075-4418
VL - 11
JO - Diagnostics
JF - Diagnostics
IS - 12
M1 - 2220
ER -