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Consequences of somatic mutations of GIRK1 detected in primary malign tumors on expression and function of G-protein activated, inwardly rectifying, K + channels.

Authors :
Pelzmann B
Hatab A
Scheruebel S
Langthaler S
Rienmueller T
Sokolowski A
Gorischek A
Platzer D
Zorn-Pauly K
Jahn SW
Bauernhofer T
Schreibmayer W
Source :
Frontiers in oncology [Front Oncol] 2022 Oct 31; Vol. 12, pp. 998907. Date of Electronic Publication: 2022 Oct 31 (Print Publication: 2022).
Publication Year :
2022

Abstract

A search in the GDC Data Portal revealed 304 documented somatic mutations of the KCNJ3 gene in primary tumors (out of 10.202 cases). Most affected tumor types were carcinomas from uterus, skin and lung, while breast cancer exerted the lowest number of somatic mutations. We focused our research on 15 missense mutations within the region between TM1 and TM2, comprising the pore helix and ion selectivity signature. Expression was measured by confocal laser scan microscopy of eGFP tagged GIRK1 subunits, expressed with and without GIRK4 in oocytes of Xenopus laevis . GIRK ion currents were activated via coexpressed m <subscript>2</subscript> Rs and measured by the Two Electrode Voltage Clamp technique. Magnitude of the total GIRK current, as well as the fraction of current inducible by the agonist, were measured. Ion selectivity was gauged by assessment of the P <subscript>Na+</subscript> /P <subscript>K+</subscript> ratio, calculated by the GIRK current reversal potential in extracellular media at different Na <superscript>+</superscript> and K <superscript>+</superscript> concentrations. None of the tested mutations was able to form functional GIRK1 homooligomeric ion channels. One of the mutations, G145A, which locates directly to the ion selectivity signature, exerted an increased P <subscript>Na+</subscript> /P <subscript>K+</subscript> ratio. Generally, the missense mutations studied can be categorized into three groups: (i) normal/reduced expression accompanied by reduced/absent function (S132Y, F136L, E139K, G145A, R149Q, R149P, G178D, S185Y, Q186R), (ii) normal/increased expression as well as increased function (E140M, A142T, M184I) and (iii) miniscule expression but increased function relative to expression levels (I151N, G158S). We conclude, that gain of function mutations, identical or similar to categories (ii) and (iii), may potentially be involved in genesis and progression of malignancies in tissues that exert a high rate of occurrence of somatic mutations of KCNJ3.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Pelzmann, Hatab, Scheruebel, Langthaler, Rienmueller, Sokolowski, Gorischek, Platzer, Zorn-Pauly, Jahn, Bauernhofer and Schreibmayer.)

Details

Language :
English
ISSN :
2234-943X
Volume :
12
Database :
MEDLINE
Journal :
Frontiers in oncology
Publication Type :
Academic Journal
Accession number :
36483038
Full Text :
https://doi.org/10.3389/fonc.2022.998907