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LNK suppresses interferon signaling in melanoma.

Abstract：

:LNK (SH2B3) is a key negative regulator of JAK-STAT signaling which has been extensively studied in malignant hematopoietic diseases. We found that LNK is significantly elevated in cutaneous melanoma; this elevation is correlated with hyperactive signaling of the RAS-RAF-MEK pathway. Elevated LNK enhances cell growth and survival in adverse conditions. Forced expression of LNK inhibits signaling by interferon-STAT1 and suppresses interferon (IFN) induced cell cycle arrest and cell apoptosis. In contrast, silencing LNK expression by either shRNA or CRISPR-Cas9 potentiates the killing effect of IFN. The IFN-LNK signaling is tightly regulated by a negative feedback mechanism; melanoma cells exposed to IFN upregulate expression of LNK to prevent overactivation of this signaling pathway. Our study reveals an unappreciated function of LNK in melanoma and highlights the critical role of the IFN-STAT1-LNK signaling axis in this potentially devastating disease. LNK may be further explored as a potential therapeutic target for melanoma immunotherapy.

journal_name

Nat Commun

journal_title

Nature communications

authors

Ding LW,Sun QY,Edwards JJ,Fernández LT,Ran XB,Zhou SQ,Scolyer RA,Wilmott JS,Thompson JF,Doan N,Said JW,Venkatachalam N,Xiao JF,Loh XY,Pein M,Xu L,Mullins DW,Yang H,Lin DC,Koeffler HP

doi

10.1038/s41467-019-09711-y

subject

Has Abstract

pub_date

2019-05-20 00:00:00

pages

2230

issue

1

issn

2041-1723

pii

10.1038/s41467-019-09711-y

journal_volume

10

pub_type

杂志文章

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