RNA interference screening methods to identify proliferation determinants and mechanisms of resistance to immune attack

Methods Enzymol. 2020:636:299-322. doi: 10.1016/bs.mie.2019.06.002. Epub 2019 Jul 3.

Abstract

We have used RNA interference (RNAi) screening technology to reveal unknown components of biological signaling pathways including survival mechanisms of estrogen-independent breast cancer cell growth and cancer cell resistance to immune attack. In this chapter, a detailed protocol describing the use of RNAi screening to identify factors important for the proliferation of estrogen-independent MCF7 breast cancer cells will be described. Resistance to therapies that target the estrogen pathway remains a challenge in the treatment of estrogen receptor-positive breast cancer. To address this challenge, small interfering-RNA (siRNA)-based libraries targeting an estrogen receptor (ER)- and aromatase-centered network, including 631 genes relevant to estrogen signaling, was designed and constructed for RNAi screening. This protocol will include the following parts: (1) selection of RNAi transfection reagent for specific cells; (2) optimization of RNAi screening conditions using Z'-factor; (3) procedure of ER-network gene siRNA library screening using automated machines under optimized experimental conditions; and (4) method of analysis for RNAi screening data to identify specific determinants important for cell proliferation. 46 genes were found to be selectively required for the survival of estrogen-independent MCF7-derived cells.

Keywords: Breast cancer; CyBio automatic dispenser; Estrogen receptor (ER); Immunotherapy; Multidrop Combi-nL reagent dispenser; RNA interference (RNAi); Screening; WellMate microplate dispenser; Z′-factor.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Breast Neoplasms* / genetics
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • MCF-7 Cells
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Receptors, Estrogen* / genetics
  • Receptors, Estrogen* / metabolism

Substances

  • RNA, Small Interfering
  • Receptors, Estrogen