Structural investigations on mechanism of lapatinib resistance caused by HER-2 mutants.

HER-2 belongs to the human epidermal growth factor receptor (HER) family. Via different signal transduction pathways, HER-2 regulates normal cell proliferation, survival, and differentiation. Recently, it was reported that MCF10A, BT474, and MDA-MB-231 cells bearing the HER2 K753E mutation were resi...

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Main Authors: Sharad Verma, Sukriti Goyal, Anchala Kumari, Aditi Singh, Salma Jamal, Abhinav Grover
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5794075?pdf=render
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author Sharad Verma
Sukriti Goyal
Anchala Kumari
Aditi Singh
Salma Jamal
Abhinav Grover
author_facet Sharad Verma
Sukriti Goyal
Anchala Kumari
Aditi Singh
Salma Jamal
Abhinav Grover
author_sort Sharad Verma
collection DOAJ
description HER-2 belongs to the human epidermal growth factor receptor (HER) family. Via different signal transduction pathways, HER-2 regulates normal cell proliferation, survival, and differentiation. Recently, it was reported that MCF10A, BT474, and MDA-MB-231 cells bearing the HER2 K753E mutation were resistant to lapatinib. Present study revealed that HER-2 mutant K753E showed some contrasting behaviour as compared to wild, L768S and V773L HER-2 in complex with lapatinib while similar to previously known lapatinib resistant L755S HER-2 mutant. Lapatinib showed stable but reverse orientation in binding site of K753E and the highest binding energy among studied HER2-lapatinib complexes but slightly lesser than L755S mutant. Results indicate that K753E has similar profile as L755S mutant for lapatinib. The interacting residues were also found different from other three studied forms as revealed by free energy decomposition and ligplot analysis.
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spelling doaj.art-41c7858cf95044e5ab48430cc310c27d2022-12-21T17:26:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01132e019094210.1371/journal.pone.0190942Structural investigations on mechanism of lapatinib resistance caused by HER-2 mutants.Sharad VermaSukriti GoyalAnchala KumariAditi SinghSalma JamalAbhinav GroverHER-2 belongs to the human epidermal growth factor receptor (HER) family. Via different signal transduction pathways, HER-2 regulates normal cell proliferation, survival, and differentiation. Recently, it was reported that MCF10A, BT474, and MDA-MB-231 cells bearing the HER2 K753E mutation were resistant to lapatinib. Present study revealed that HER-2 mutant K753E showed some contrasting behaviour as compared to wild, L768S and V773L HER-2 in complex with lapatinib while similar to previously known lapatinib resistant L755S HER-2 mutant. Lapatinib showed stable but reverse orientation in binding site of K753E and the highest binding energy among studied HER2-lapatinib complexes but slightly lesser than L755S mutant. Results indicate that K753E has similar profile as L755S mutant for lapatinib. The interacting residues were also found different from other three studied forms as revealed by free energy decomposition and ligplot analysis.http://europepmc.org/articles/PMC5794075?pdf=render
spellingShingle Sharad Verma
Sukriti Goyal
Anchala Kumari
Aditi Singh
Salma Jamal
Abhinav Grover
Structural investigations on mechanism of lapatinib resistance caused by HER-2 mutants.
PLoS ONE
title Structural investigations on mechanism of lapatinib resistance caused by HER-2 mutants.
title_full Structural investigations on mechanism of lapatinib resistance caused by HER-2 mutants.
title_fullStr Structural investigations on mechanism of lapatinib resistance caused by HER-2 mutants.
title_full_unstemmed Structural investigations on mechanism of lapatinib resistance caused by HER-2 mutants.
title_short Structural investigations on mechanism of lapatinib resistance caused by HER-2 mutants.
title_sort structural investigations on mechanism of lapatinib resistance caused by her 2 mutants
url http://europepmc.org/articles/PMC5794075?pdf=render
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