» Articles » PMID: 37354211

Expression, Prognostic Value and Mechanism of SP100 Family in Pancreatic Adenocarcinoma

Overview
Specialty Geriatrics
Date 2023 Jun 24
PMID 37354211
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Pancreatic adenocarcinoma (PAAD) is one of the most aggressive malignancies with a very poor prognosis. Exploring more therapeutic targets and prognostic biomarkers is of great significance to improve the prognosis of PAAD patients. Increasing evidence supports that the speckled protein (SP) 100 family is associated with human cancer and immune disorders. However, the function of the SP100 family members in PAAD is still unclear.

Methods: R, Cytoscape, cBioPortal, and other software and online databases were used to comprehensively analyze the expression characteristics, prognostic value, and oncogenic mechanism of the SP100 family in PAAD.

Results: The high expression of SP100 family members in PAAD was significantly correlated with poor clinicopathological features and poor prognosis of PAAD patients. Mechanistically, TP53 mutations were significantly associated with the expression levels of the SP100 family members, which were significantly coexpressed with M6A methylation regulators and were activated in multiple oncogenic pathways, including the EMT pathways. Moreover, we found that their expression levels were significantly correlated with the sensitivity of multiple traditional chemotherapeutic drugs.

Conclusion: The SP100 family is closely related to the occurrence and development of PAAD and can be used as a new biomarker and therapeutic target for patients with PAAD.

Citing Articles

Discovery of novel serum peptide biomarkers for cholangiocarcinoma recurrence through MALDI-TOF MS and LC-MS/MS peptidome analysis.

Thanasukarn V, Prajumwongs P, Muangritdech N, Loilome W, Namwat N, Klanrit P Sci Rep. 2025; 15(1):2582.

PMID: 39833435 PMC: 11746940. DOI: 10.1038/s41598-025-87124-2.


An investigation of the molecular characterization of the tripartite motif (TRIM) family and primary validation of TRIM31 in gastric cancer.

Ding Y, Lu Y, Guo J, Chen S, Han X, Wang S Hum Genomics. 2024; 18(1):77.

PMID: 38978046 PMC: 11232234. DOI: 10.1186/s40246-024-00631-7.


SP140 inhibitor suppressing TRIM22 expression regulates glioma progress through PI3K/AKT signaling pathway.

Li X, Li G, Li L, Gao B, Niu X, Wang Y Brain Behav. 2024; 14(3):e3465.

PMID: 38468469 PMC: 10928341. DOI: 10.1002/brb3.3465.

References
1.
Tanabe A, Tanikawa K, Tsunetomi M, Takai K, Ikeda H, Konno J . RNA helicase YTHDC2 promotes cancer metastasis via the enhancement of the efficiency by which HIF-1α mRNA is translated. Cancer Lett. 2016; 376(1):34-42. DOI: 10.1016/j.canlet.2016.02.022. View

2.
Zhang C, Huang S, Zhuang H, Ruan S, Zhou Z, Huang K . YTHDF2 promotes the liver cancer stem cell phenotype and cancer metastasis by regulating OCT4 expression via m6A RNA methylation. Oncogene. 2020; 39(23):4507-4518. DOI: 10.1038/s41388-020-1303-7. View

3.
Zhuang H, Chen X, Dong F, Zhang Z, Zhou Z, Ma Z . Prognostic values and immune suppression of the S100A family in pancreatic cancer. J Cell Mol Med. 2021; 25(6):3006-3018. PMC: 7957204. DOI: 10.1111/jcmm.16343. View

4.
Wang M, Liu J, Zhao Y, He R, Xu X, Guo X . Upregulation of METTL14 mediates the elevation of PERP mRNA N adenosine methylation promoting the growth and metastasis of pancreatic cancer. Mol Cancer. 2020; 19(1):130. PMC: 7446161. DOI: 10.1186/s12943-020-01249-8. View

5.
Du Y, Liu Z, You L, Hou P, Ren X, Jiao T . Pancreatic Cancer Progression Relies upon Mutant p53-Induced Oncogenic Signaling Mediated by NOP14. Cancer Res. 2017; 77(10):2661-2673. DOI: 10.1158/0008-5472.CAN-16-2339. View