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.
引用
收藏
页数:10
相关论文
共 50 条
  • [21] THREE SPLICE VARIANTS OF OSTEOPONTIN IN HUMAN LUNG CANCER, EXPRESSION PATTERN AND CLINICAL/PROGNOSTIC RELEVANCE
    Hao, Chengcheng
    Zhang, Lijian
    Du, Guifang
    Gu, Yanan
    He, Junqi
    Cheng, Shan
    Jiang, Wen G.
    ANTICANCER RESEARCH, 2015, 35 (07) : 4347 - 4347
  • [22] Osteopontin-c splicing isoform is a key molecule in ovarian cancer progression
    Tilli, Tatiana M.
    Mello, Kivvi D.
    Franco, Vanessa
    Robbs, Bruno
    Wanderley, Joao Luiz
    Rass, Fabricio
    Viola, Joao P. B.
    Weber, Georg
    Castronovo, Vincent
    Bellahcene, Akeila
    Gimba, Etel R. P.
    Gimba, Etel
    CLINICAL CANCER RESEARCH, 2013, 19
  • [23] Changes in the transcriptional profile in response to overexpression of the osteopontin-c splice isoform in ovarian (OvCar-3) and prostate (PC-3) cancer cell lines
    Tilli, Tatiana M.
    Bellahcene, Akeila
    Castronovo, Vincent
    Gimba, Etel R. P.
    BMC CANCER, 2014, 14
  • [24] Osteopontin-c and Osteopontin-b splicing isoforms activate important hallmarks of cancer contributing to prostate carcinoma progression
    Tilli, Tatiana M.
    Matos, Aline
    Goulart, Luis Ricardo
    Weber, Georg F.
    Pereira Gimba, Etel Rodrigues
    CANCER RESEARCH, 2011, 71
  • [25] Changes in the transcriptional profile in response to overexpression of the osteopontin-c splice isoform in ovarian (OvCar-3) and prostate (PC-3) cancer cell lines
    Tatiana M Tilli
    Akeila Bellahcène
    Vincent Castronovo
    Etel R P Gimba
    BMC Cancer, 14
  • [26] Osteopontin splice variants are differential predictors of breast cancer treatment responses
    Krzysztof Zduniak
    Anil Agrawal
    Siddarth Agrawal
    Md Monir Hossain
    Piotr Ziolkowski
    Georg F. Weber
    BMC Cancer, 16
  • [27] Osteopontin splice variants are differential predictors of breast cancer treatment responses
    Zduniak, Krzysztof
    Agrawal, Anil
    Agrawal, Siddarth
    Hossain, Md Monir
    Ziolkowski, Piotr
    Weber, Georg F.
    BMC CANCER, 2016, 16
  • [28] Tertiary structure prediction and identification of druggable pocket in the cancer biomarker - Osteopontin-c
    Sivakumar S.
    Niranjali Devaraj S.
    Journal of Diabetes & Metabolic Disorders, 13 (1):
  • [29] Both osteopontin-c and osteopontin-b splicing isoforms exert pro-tumorigenic roles in prostate cancer cells
    Tilli, Tatiana M.
    Mello, Kivvi D.
    Ferreira, Luciana B.
    Matos, Aline R.
    Accioly, Maria Thereza S.
    Faria, Paulo A. S.
    Bellahcene, Akeila
    Castronovo, Vincent
    Gimba, Etel R.
    PROSTATE, 2012, 72 (15): : 1688 - 1699
  • [30] Prognostic impact of mRNA levels of osteopontin splice variants in soft tissue sarcoma patients
    Hahnel, Antje
    Wichmann, Henri
    Greither, Thomas
    Kappler, Matthias
    Wuerl, Peter
    Kotzsch, Matthias
    Taubert, Helge
    Vordermark, Dirk
    Bache, Matthias
    BMC CANCER, 2012, 12