Quantitative proteomics identifies myoferlin as a novel regulator of A Disintegrin and Metalloproteinase 12 in HeLa cells

J Proteomics. 2016 Oct 4:148:94-104. doi: 10.1016/j.jprot.2016.07.015. Epub 2016 Jul 16.

Abstract

A Disintegrin and Metalloproteinase 12 (ADAM12) is expressed significantly higher in multiple tumors than in normal tissues and has been used as a prognostic marker for the evaluation of cancer progression. Although several ADAM12 substrates have been identified biochemically and its proteolytic function has been explored, the upstream regulators and the interacting proteins have not been systematically investigated. Here, we use immunoprecipitation and mass spectrometry (MS)-based quantitative proteomic approaches to identify 28 interacting partners for the long form of ADAM12 (ADAM12-L) in HeLa cells. Proteins that regulate cell proliferation, invasion, and epithelial to mesenchymal transition are among the identified ADAM12-interacting proteins. Further biochemical experiments discover that the protein level and the stability of ADAM12 are upregulated by one of its interacting proteins, myoferlin. In addition, myoferlin also increases the proteolytic activity of ADAM12, leading to the reduction of an ADAM12 substrate, E-cadherin. This result implies that ADAM12 and its interacting proteins might converge to certain signaling pathways in the regulation of cancer cell progression. The information obtained here might be useful in the development of new strategies for modulating cell proliferation and invasion involved in the regulation between ADAM12 and its interacting partners. MS data are available via ProteomeXchange with identifier PXD003560.

Biological significance: Regulation of the proliferation and invasion of cancer cells is important in cancer treatment. ADAM12 has been found to play important roles in regulating these processes and identification of its interacting partners will improve our understanding of its biological functions and provide basis for functional modulation. Through mass spectrometry-based quantitative proteomic approaches, we identify the interacting partners for ADAM12 in a human cancer cell line and find many proteins that are involved in the proliferation and invasion of cancer cells. A novel regulator, myoferlin, of ADAM12 is discovered and this protein increases ADAM12 expression level, stability, and its enzymatic activity, leading to the reduction of its substrate, E-cadherin, which plays important roles in the regulation of cell adhesion and tumor metastasis. This result provides a connection for two highly expressed proteins in cancer cells and may shed light on the regulation of their biological functions in cancer progression.

Keywords: ADAM12; E-cadherin; Label-free; Myoferlin; Quantitative proteomics; Spectral counting.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM12 Protein / analysis
  • ADAM12 Protein / metabolism*
  • Cadherins / analysis
  • Cadherins / metabolism*
  • Calcium-Binding Proteins / analysis
  • Calcium-Binding Proteins / isolation & purification
  • Calcium-Binding Proteins / physiology*
  • Cell Line, Tumor
  • Cell Proliferation
  • Disease Progression
  • Gene Expression Regulation, Neoplastic
  • HeLa Cells
  • Humans
  • Membrane Proteins / analysis
  • Membrane Proteins / isolation & purification
  • Membrane Proteins / physiology*
  • Muscle Proteins / analysis
  • Muscle Proteins / isolation & purification
  • Muscle Proteins / physiology*
  • Neoplasm Invasiveness
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Protein Interaction Maps*
  • Proteomics / methods*

Substances

  • Cadherins
  • Calcium-Binding Proteins
  • MYOF protein, human
  • Membrane Proteins
  • Muscle Proteins
  • ADAM12 Protein
  • ADAM12 protein, human