From Malignant Progression to Therapeutic Targeting: Current Insights of Mesothelin in Pancreatic Ductal Adenocarcinoma

Int J Mol Sci. 2020 Jun 6;21(11):4067. doi: 10.3390/ijms21114067.

Abstract

Pancreatic ductal adenocarcinoma (PDAC), accounting for 90% of all pancreatic tumors, is a highly devastating disease with poor prognosis and rising incidence. The lack of available specific diagnostics tests and the limited treatment opportunities contribute to this pejorative issue. Over the last 10 years, a growing interest pointing towards mesothelin (MSLN) as a promising PDAC-associated antigen has emerged. The limited expression of MSLN in normal tissues (peritoneum, pleura and pericardium) and its overexpression in 80 to 90% of PDAC make it an attractive candidate for therapeutic management of PDAC patients. Moreover, its role in malignant progression related to its involvement in tumor cell proliferation and resistance to chemotherapy has highlighted the relevance of its targeting. Hence, several clinical trials are investigating anti-MSLN efficacy in PDAC. In this review, we provide a general overview of the different roles sustained by MSLN during PDAC progression. Finally, we also summarize the different MSLN-targeted therapies that are currently tested in the clinic.

Keywords: CAR T-cells; PDAC; antibody-based therapy; mesothelin; vaccines.

Publication types

  • Review

MeSH terms

  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / immunology
  • Antigens, Neoplasm / metabolism
  • Apoptosis
  • Biomarkers, Tumor
  • Cancer Vaccines / therapeutic use
  • Carcinoma, Pancreatic Ductal / diagnosis
  • Carcinoma, Pancreatic Ductal / etiology*
  • Carcinoma, Pancreatic Ductal / therapy*
  • Cell Proliferation
  • Combined Modality Therapy
  • Disease Management
  • Disease Progression
  • Disease Susceptibility
  • Drug Development
  • GPI-Linked Proteins / genetics*
  • GPI-Linked Proteins / immunology
  • GPI-Linked Proteins / metabolism
  • Humans
  • Mesothelin
  • Molecular Targeted Therapy
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Pancreatic Neoplasms / diagnosis
  • Pancreatic Neoplasms / immunology*
  • Pancreatic Neoplasms / therapy*
  • Prognosis

Substances

  • Antigens, Neoplasm
  • Biomarkers, Tumor
  • Cancer Vaccines
  • GPI-Linked Proteins
  • MSLN protein, human
  • Mesothelin