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. 2013 Sep 1;119(17):3148-55.
doi: 10.1002/cncr.28144. Epub 2013 May 29.

Pronecrotic mixed lineage kinase domain-like protein expression is a prognostic biomarker in patients with early-stage resected pancreatic adenocarcinoma

Affiliations

Pronecrotic mixed lineage kinase domain-like protein expression is a prognostic biomarker in patients with early-stage resected pancreatic adenocarcinoma

Lauren E Colbert et al. Cancer. .

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.

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Conflict of interest statement

Conflict of interest disclosures: the authors made no disclosures.

Figures

Figure 1
Figure 1
Kaplan-Meier log-rank survival analysis for mixed lineage kinase domain-like protein (MLKL) expression in patients undergoing adjuvant therapy (n = 59) is shown, demonstrating the extreme outliers found in the group of patients with the lowest MLKL expression (those with an expression score < 1).
Figure 2
Figure 2
Immunohistochemical expression of mixed lineage kinase domain-like protein (MLKL) in tumor tissue is shown. The intensity of the cytoplasmic expression of MLKL in tumor cells was graded as (A) low, (B) medium, or (C) high.
Figure 3
Figure 3
Kaplan-Meier log-rank survival analysis is shown for mixed lineage kinase domain-like protein (MLKL) expression in all patients (n = 80). (A) The effect of MLKL expression on recurrence-free survival is shown. (B) The effect of MLKL expression on overall survival is shown.
Figure 4
Figure 4
Kaplan-Meier log-rank survival analysis for mixed lineage kinase domain-like protein (MLKL) expression is shown in patients receiving adjuvant therapy (n = 59). (A) The effect of MLKL expression on recurrence-free survival is shown. (B) The effect of MLKL expression on overall survival is shown.
Figure 5
Figure 5
Kaplan-Meier log-rank survival analysis for mixed lineage kinase domain-like protein (MLKL) expression is shown in patients receiving gemcitabine therapy (n = 32). (A) The effect of MLKL expression on recurrence-free survival is shown. (B) The effect of MLKL expression on overall survival is shown.

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