Detection of Retinoblastoma Protein Phosphorylation by Immunoblot Analysis

Methods Mol Biol. 2018:1726:49-64. doi: 10.1007/978-1-4939-7565-5_6.

Abstract

The retinoblastoma tumor suppressor protein (pRb) is a preeminent tumor suppressor that acts as a cell cycle repressor, specifically as an inhibitor of the G1-S transition of the cell cycle . pRb is a phosphoprotein whose function is repressed by extensive phosphorylation in several key residues, and therefore, pRb's phosphorylation status has become a surrogate for pRb activity. In particular, hyperphosphorylation of pRb has been associated with pathological states such as cancer, and therefore, assessing pRb's phosphorylation status is increasingly gaining diagnostic and prognostic value, may be used to inform therapeutic decisions, and is also an important tool for the cancer biologists seeking an understanding of the molecular etiology of cancer. In this chapter, we discuss an immunoblot protocol to detect pRb phosphorylation in two residues, serine 612 and threonine 821, in protein extracts from cancer cells.

Keywords: Cell cycle control; Immunoblot; Lung adenocarcinoma; Oncogenesis; Phosphorylation; Retinoblastoma protein.

MeSH terms

  • Cell Cycle Proteins / metabolism
  • Humans
  • Immunoblotting / methods*
  • Neoplasms / diagnosis*
  • Neoplasms / metabolism
  • Phosphorylation
  • Retinoblastoma Binding Proteins / metabolism*
  • Tumor Cells, Cultured
  • Ubiquitin-Protein Ligases / metabolism*

Substances

  • Cell Cycle Proteins
  • RB1 protein, human
  • Retinoblastoma Binding Proteins
  • Ubiquitin-Protein Ligases