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. 2014 Dec 23;9(12):e115600. doi: 10.1371/journal.pone.0115600

Table 1. Panel of cell radiosensitivity and mutation status.

Cell Line SF2 KRas p53 Keap1
HBEC 3KT 0.487 wt wt wt
HBEC 3KT + KRas V12 0.474 X wt wt
HBEC 3KT + KRas V12 +sh p53 0.650 X X wt
HBEC 3KT + KRasV12 +sh p53 + myc 0.702 X X wt
HBEC 30KT 0.442 wt wt -
HCC 4017 0.321 mut mut (C833A) wt
A549 0.771 mut (G34A) wt mut (G333C);constitutive Nrf2 activation
H2009 0.615 mut (G35C) mut (G818T) wt
HCC 2429 0.514 wt mut (G800A) wt
HCC 15 0.484 wt mut (A776T) wt
H23 0.053 mut mut mut; Nrf2 still inducible
HME1 0.528 wt wt wt
HMEC 50 0.659 wt mut -
MDA-MB-231 0.452 mut (G38A) mut (G839A) wt

A summary of all cell lines used in the present study. Surviving fraction of cells at 2 Gy (SF2) is used as a metric of radio-sensitivity, with SF2>0.6 considered a “resistant” line and SF2<0.4 considered a “sensitive” line. Mutation status of KRas, p53, and Keap1/Nrf2 is listed as either wildtype (wt) or mutated (mut) as determined by full exon sequencing (John Minna and Adi Gazdar, UT-Southwestern Medical Center, Dallas, TX, personal communications). A mutation is present in Keap1 in the NSCLC H23 cell line (personal communications with Brandon Probst, Reata Pharmaceuticals). “X” indicates experimentally manipulated gene expression.