Overexpression of Osteopontin-a and Osteopontin-c Splice Variants Are Worse Prognostic Features in Colorectal Cancer

被引:1
|
作者
Mattos, Daniella [1 ,2 ]
Rocha, Murilo [3 ]
Tessmann, Josiane [3 ]
Ferreira, Luciana [1 ,4 ]
Gimba, Etel [1 ,2 ,5 ]
机构
[1] Natl Inst Canc, Hematooncol Mol Program, 23rd Red Cross Sq,6th Floor, BR-20230130 Rio De Janeiro, RJ, Brazil
[2] Fluminense Fed Univ, Biomed Sci Grad Program, Rua Prof Hernani Pires de Melo 101, BR-24210130 Niteroi, RJ, Brazil
[3] Natl Inst Canc, Cellular & Mol Oncobiol Program, BR-20231050 Rio De Janeiro, RJ, Brazil
[4] Univ Fed Rural Rio de Janeiro, Dept Genet, Inst Ciencias Biol & Saude, BR 465,Km 07, BR-23897000 Rio De Janeiro, RJ, Brazil
[5] Fluminense Fed Univ, Humanities & Hlth Inst, Dept Ciencias Nat, Recife St, BR-28895532 Rio Das Ostras, RJ, Brazil
关键词
osteopontin; colorectal cancer; splice variants; PAPILLARY THYROID-CARCINOMA; 1ST-LINE TREATMENT; BRAF MUTATION; EXPRESSION; SURVIVAL; CETUXIMAB; TARGET; GENE; KRAS;
D O I
10.3390/diagnostics14192108
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Osteopontin (OPN) is a glycoprotein involved in various physiological and pathological processes, and its aberrant expression in cancer cells is closely linked to tumor progression. In colorectal cancer (CRC), OPN is overexpressed, but the roles of its splice variants (OPN-SVs), OPNa, OPNb, and OPNc, are not well understood. This study aimed to characterize the expression patterns of OPN-SVs and their potential diagnostic and prognostic implications in CRC using transcriptomic data deposited in TSVdb and TCGA. Methods: The expression patterns of each OPN-SV were analyzed using transcriptomic data deposited in TSVdb and TCGA, which were correlated to patient data available at cBioPortal. Results: Bioinformatic analysis revealed that OPNa, OPNb, and OPNc are overexpressed in CRC samples compared to non-tumor samples. Notably, OPNa and OPNc are overexpressed in CRC stages (II, III, and IV) compared to stage I. Higher levels of OPNa and OPNc transcripts are associated with worse overall survival (OS) and shorter progression-free survival (PFS) in CRC patients. Additionally, the expression of OPNa, OPNb, and OPNc is correlated with BRAFV600E mutations in CRC samples. Conclusions: These findings suggest that OPNa and OPNc, in particular, have potential as diagnostic and prognostic biomarkers, paving the way for their further evaluation in CRC diagnosis and prognosis.
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页数:10
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