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. 2023 Jan 31;26(2):106096. doi: 10.1016/j.isci.2023.106096

Table 1.

General description of the eight MPNST cell lines analyzed

S462 ST88-14 NF90-8 sNF96.2 NMS-2 STS-26T HS-Sch-2 HS-PSS
Type of human MPNST primary, grade IV primary primary, from PNF primary primary metastasis, grade III/III primary, low grade UNK
MPNST localization thigh retroperitoneum left forearm leg right thigh left scapula left thigh prostate
NF1/Sp NF1 NF1 NF1 NF1 NF1 Sp Sp Sp
Age of patient 19 24 17 27 30 51 54 UNK
Sex of patient F M F M M F F M
Original Reference Frahm-2004 Fletcher-1991 Legius-1994 Perrin-2007 Imaizumi-1998 Dahlberg-1993 Sonobe-2000 n/a
NF1 constitutional pathogenic variant c.6855C>A p.Y2264X Frahm-2004 c.1649dupT p.V551Gfs∗7 Varin-2016 c.3904_3910del p.D1302Yfs∗5 Wu-1999 c.3683delC p.N1229Mfs∗11 Perrin-2007 c.6999+1G>T (splice donor)
NF1 somatic pathogenic variant LOH LOH LOH LOH LOH LOH c.270_288del
p.E91Nfs∗6; c.3113+1G>A (splice donor)

MPNST: Malignant peripheral nerve sheath tumor; NF1/Sp: NF1-related/Sporadic MPNST; F:Female; M: Male; Bold annotations: mutations described in this article; LOH: Loss of Heterozygosity; UNK: Unknown.