Pronecrotic mixed lineage kinase domain-like protein expression is a prognostic biomarker in patients with early-stage resected pancreatic adenocarcinoma
- PMID: 23720157
- PMCID: PMC4389890
- DOI: 10.1002/cncr.28144
Pronecrotic mixed lineage kinase domain-like protein expression is a prognostic biomarker in patients with early-stage resected pancreatic adenocarcinoma
Abstract
Background: Mixed lineage kinase domain-like protein (MLKL) is a necrosome component mediating programmed necrosis that may be an important determinant of cancer cell death. The goal of the current study was to evaluate the prognostic value of MLKL expression in patients with pancreatic adenocarcinoma (PAC).
Methods: Tissue from 80 patients was collected from a prospectively maintained database of patients with PAC who underwent pancreaticoduodenectomy between January 2000 and October 2008. Immunohistochemistry analysis was performed and scored using an established scoring system. Kaplan-Meier survival curves were generated for recurrence-free survival (RFS) and overall survival (OS) for all patients and for patients receiving adjuvant chemotherapy. MLKL scores were correlated with RFS and OS using univariate and multivariate Cox regression analyses incorporating clinically relevant covariates.
Results: The median age of the patients was 63 years and 53% were men. Low MLKL expression was associated with decreased OS (6 months vs 17 months; P = .006). In the subset of 59 patients who received adjuvant chemotherapy, low MLKL expression was associated with decreased RFS (5 months vs 15 months; P = .006) and decreased OS (6 months vs 19 months; P < .0001). On multivariate analysis, low MLKL expression was associated with poor OS in all patients (hazards ratio, 4.6 [95% confidence interval, 1.6-13.8]; P = .006) and in patients receiving adjuvant chemotherapy (hazards ratio, 8.1 [95% confidence interval, 2.2-29.2]; P = .002).
Conclusions: Low expression of MLKL is associated with decreased OS in patients with resected PAC and decreased RFS and OS in the subset of patients with resected PAC who receive adjuvant chemotherapy. The use of this biomarker in patients with PAC may provide important prognostic information.
Keywords: biomarker; mixed lineage kinase domain-like protein (MLKL); necroptosis; necrosis; pancreatic cancer.
Copyright © 2013 American Cancer Society.
Conflict of interest statement
Conflict of interest disclosures: the authors made no disclosures.
Figures
Similar articles
-
Association of Mixed Lineage Kinase Domain-Like Protein Expression With Prognosis in Patients With Colon Cancer.Technol Cancer Res Treat. 2017 Aug;16(4):428-434. doi: 10.1177/1533034616655909. Epub 2016 Jul 18. Technol Cancer Res Treat. 2017. PMID: 27432118 Free PMC article.
-
Differential expression and prognostic value of ERCC1 and thymidylate synthase in resected gastric adenocarcinoma.Cancer. 2013 Sep 1;119(17):3242-50. doi: 10.1002/cncr.28175. Epub 2013 May 29. Cancer. 2013. PMID: 23719746 Free PMC article.
-
An analysis of human equilibrative nucleoside transporter-1, ribonucleoside reductase subunit M1, ribonucleoside reductase subunit M2, and excision repair cross-complementing gene-1 expression in patients with resected pancreas adenocarcinoma: implications for adjuvant treatment.Cancer. 2013 Jan 15;119(2):445-53. doi: 10.1002/cncr.27619. Epub 2012 May 8. Cancer. 2013. PMID: 22569992
-
Differential expression of ERCC1 in pancreas adenocarcinoma: high tumor expression is associated with earlier recurrence and shortened survival after resection.Ann Surg Oncol. 2011 Sep;18(9):2699-705. doi: 10.1245/s10434-011-1610-x. Epub 2011 Mar 1. Ann Surg Oncol. 2011. PMID: 21360249
-
Clinical characteristics of early onset pancreatic adenocarcinoma: a medical center experience and review of the literature.Pancreas. 2011 May;40(4):638-9. doi: 10.1097/MPA.0b013e318214fe56. Pancreas. 2011. PMID: 21483255 Review. No abstract available.
Cited by
-
The potential role of necroptosis in clinical diseases (Review).Int J Mol Med. 2021 May;47(5):89. doi: 10.3892/ijmm.2021.4922. Epub 2021 Mar 31. Int J Mol Med. 2021. PMID: 33786617 Free PMC article. Review.
-
From (Tool)Bench to Bedside: The Potential of Necroptosis Inhibitors.J Med Chem. 2023 Feb 23;66(4):2361-2385. doi: 10.1021/acs.jmedchem.2c01621. Epub 2023 Feb 13. J Med Chem. 2023. PMID: 36781172 Free PMC article. Review.
-
Necroptosis pathways in tumorigenesis.Semin Cancer Biol. 2022 Nov;86(Pt 3):32-40. doi: 10.1016/j.semcancer.2022.07.007. Epub 2022 Jul 28. Semin Cancer Biol. 2022. PMID: 35908574 Free PMC article. Review.
-
Regulation of alveolar macrophage death in acute lung inflammation.Respir Res. 2018 Mar 27;19(1):50. doi: 10.1186/s12931-018-0756-5. Respir Res. 2018. PMID: 29587748 Free PMC article. Review.
-
MLKL inhibits intestinal tumorigenesis by suppressing STAT3 signaling pathway.Int J Biol Sci. 2021 Feb 17;17(3):869-881. doi: 10.7150/ijbs.56152. eCollection 2021. Int J Biol Sci. 2021. PMID: 33767595 Free PMC article.
References
-
- Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012. CA Cancer J Clin. 2012;62:10–29. - PubMed
-
- Oettle H, Post S, Neuhaus P, et al. Adjuvant chemotherapy with gemcitabine vs observation in patients undergoing curative-intent resection of pancreatic cancer: a randomized controlled trial. JAMA. 2007;297:267–277. - PubMed
-
- Heinemann V, Haas M, Boeck S. Systemic treatment of advanced pancreatic cancer. Cancer Treat Rev. 2012;38:843–853. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous