» Articles » PMID: 35547358

A Computational Approach to Justifying Stratifin As a Candidate Diagnostic and Prognostic Biomarker for Pancreatic Cancer

Abstract

Pancreatic cancer (PC) is considered a silent killer because it does not show specific symptoms at an early stage. Thus, identifying suitable biomarkers is important to avoid the burden of PC. Stratifin (SFN) encodes the 14-3-3 protein, which is expressed in a tissue-dependent manner and plays a vital role in cell cycle regulation. Thus, SFN could be a promising therapeutic target for several types of cancer. This study was aimed at investigating, using online bioinformatics tools, whether SFN could be used as a diagnostic and prognostic biomarker in PC. SFN expression was explored by utilizing the ONCOMINE, UALCAN, GEPIA2, and GENT2 tools, which revealed that SFN expression is higher in PC than in normal tissues. The clinicopathological analysis using the ULCAN tool showed that the intensity of SFN expression is commensurate with cancer progression. GEPIA2, R2, and OncoLnc revealed a negative correlation between SFN expression and survival probability in PC patients. The ONCOMINE, UCSC Xena, and GEPIA2 tools showed that cofilin 1 is strongly coexpressed with SFN. Moreover, enrichment and network analyses of SFN were performed using the Enrichr and NetworkAnalyst platforms, respectively. Receiver operating characteristic (ROC) curves revealed that tissue-dependent expression of the SFN gene could serve as a diagnostic and prognostic biomarker. However, further wet laboratory studies are necessary to determine the relevance of SFN expression as a biomarker.

Citing Articles

GPR55 in the tumor microenvironment of pancreatic cancer controls tumorigenesis.

Ristic D, Barnthaler T, Gruden E, Kienzl M, Danner L, Herceg K Front Immunol. 2025; 15:1513547.

PMID: 39885986 PMC: 11779727. DOI: 10.3389/fimmu.2024.1513547.


Lymph Node Metastasis in Gastrointestinal Carcinomas: A View from a Proteomics Perspective.

Jain V, Sakhuja P, Agarwal A, Sirdeshmukh R, Siraj F, Gautam P Curr Oncol. 2024; 31(8):4455-4475.

PMID: 39195316 PMC: 11352871. DOI: 10.3390/curroncol31080333.


Integrated bioinformatics analysis reveals upregulated extracellular matrix hub genes in pancreatic cancer: Implications for diagnosis, prognosis, immune infiltration, and therapeutic strategies.

Mogal M, Jame J, Sohel M, Mozibullah M, Mahmod M, Junayed A Cancer Rep (Hoboken). 2024; 7(4):e2059.

PMID: 38639039 PMC: 11027013. DOI: 10.1002/cnr2.2059.


Genetic Signature of Human Pancreatic Cancer and Personalized Targeting.

Reshkin S, Cardone R, Koltai T Cells. 2024; 13(7.

PMID: 38607041 PMC: 11011857. DOI: 10.3390/cells13070602.

References
1.
Lachmann A, Xu H, Krishnan J, Berger S, Mazloom A, Maayan A . ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experiments. Bioinformatics. 2010; 26(19):2438-44. PMC: 2944209. DOI: 10.1093/bioinformatics/btq466. View

2.
Rhodes D, Kalyana-Sundaram S, Mahavisno V, Varambally R, Yu J, Briggs B . Oncomine 3.0: genes, pathways, and networks in a collection of 18,000 cancer gene expression profiles. Neoplasia. 2007; 9(2):166-80. PMC: 1813932. DOI: 10.1593/neo.07112. View

3.
Turanli B, Yildirim E, Gulfidan G, Arga K, Sinha R . Current State of "Omics" Biomarkers in Pancreatic Cancer. J Pers Med. 2021; 11(2). PMC: 7918884. DOI: 10.3390/jpm11020127. View

4.
Klamt F, Zdanov S, Levine R, Pariser A, Zhang Y, Zhang B . Oxidant-induced apoptosis is mediated by oxidation of the actin-regulatory protein cofilin. Nat Cell Biol. 2009; 11(10):1241-6. PMC: 3393095. DOI: 10.1038/ncb1968. View

5.
Rhodes D, Yu J, Shanker K, Deshpande N, Varambally R, Ghosh D . ONCOMINE: a cancer microarray database and integrated data-mining platform. Neoplasia. 2004; 6(1):1-6. PMC: 1635162. DOI: 10.1016/s1476-5586(04)80047-2. View