@article{a269941421cb483287659c05604feffb,
title = "Expression profiles and prognostic value of FABPs in colorectal adenocarcinomas",
abstract = "Colorectal cancer (CRC) is one of the world{\textquoteright}s leading causes of cancer-related deaths; thus, it is important to detect it as early as possible. Obesity is thought to be linked to a large rise in the CRC incidence as a result of bad dietary choices, such as a high intake of animal fats. Fatty acid-binding proteins (FABPs) are a set of molecules that coordinate intracellular lipid responses and are highly associated with metabolism and inflammatory pathways. There are nine types of FABP genes that have been found in mammals, which are FABP1–7, FABP9, and FABP12. Each FABP gene has its own roles in different organs of the body; hence, each one has different expression levels in different cancers. The roles of FABP family genes in the development of CRC are still poorly understood. We used a bioinformatics approach to examine FABP family gene expression profiles using the Oncomine, GEPIA, PrognoScan, STRING, cBioPortal, MetaCore, and TIMER platforms. Results showed that the FABP6 messenger (m)RNA level is overexpressed in CRC cells compared to normal cells. The overexpression of FABP6 was found to be related to poor prognosis in CRC patients{\textquoteright} overall survival. The immunohistochemical results in the Human Protein Atlas showed that FABP1 and FABP6 exhibited strong staining in CRC tissues. An enrichment analysis showed that high expression of FABP6 was significantly correlated with the role of microRNAs in cell proliferation in the development of CRC through the insulin-like growth factor (IGF) signaling pathway. FABP6 functions as an intracellular bile-acid transporter in the ileal epithelium. We looked at FABP6 expression in CRC since bile acids are important in the carcinogenesis of CRC. In conclusion, high FABP6 expression is expected to be a potential biomarker for detecting CRC at the early stage.",
keywords = "Bioinformatics, Colorectal cancer, FABP family genes, FABP6, Prognosis",
author = "Prayugo, {Fidelia Berenice} and Kao, {Tzu Jen} and Gangga Anuraga and Ta, {Hoang Dang Khoa} and Chuang, {Jian Ying} and Lin, {Li Chia} and Wu, {Yung Fu} and Wang, {Chih Yang} and Lee, {Kuen Haur}",
note = "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-C03-03 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: {\textcopyright} 2021 by the authors. Licensee MDPI, Basel, Switzerland.",
year = "2021",
month = oct,
doi = "10.3390/biomedicines9101460",
language = "English",
volume = "9",
journal = "Biomedicines",
issn = "2227-9059",
publisher = "MDPI AG",
number = "10",
}