Three members of transmembrane-4-superfamily, tm4sf1, Tm4sf4, and tm4sf5, as emerging anticancer molecular Targets against cancer phenotypes and chemoresistance

There are six members of the transmembrane 4 superfamily (TM4SF) that have similar topology and sequence homology. Physiologically, they regulate tissue differentiation, signal transduction pathways, cellular activation, proliferation, motility, adhesion, and angiogenesis. Accumulating evidence has...

Full description

Bibliographic Details
Main Authors: Nur Syafiqah Rahim, Yuan Seng Wu, Maw Shin Sim, Appalaraju Velaga, Srinivasa Reddy Bonam, Subash C. B. Gopinath, Vetriselvan Subramaniyan, Ker Woon Choy, Sin-Yeang Teow, Ismail M. Fareez, Chandramathi Samudi, Shamala Devi Sekaran, Mahendran Sekar, Rhanye Mac Guad
Format: Article
Language:English
English
Published: Molecular Diversity Preservation International (MDPI) 2023
Subjects:
Online Access:https://eprints.ums.edu.my/id/eprint/35751/1/ABSTRACT.pdf
https://eprints.ums.edu.my/id/eprint/35751/2/FULL%20%20TEXT.pdf
_version_ 1825715245133332480
author Nur Syafiqah Rahim
Yuan Seng Wu
Maw Shin Sim
Appalaraju Velaga
Srinivasa Reddy Bonam
Subash C. B. Gopinath
Vetriselvan Subramaniyan
Ker Woon Choy
Sin-Yeang Teow
Ismail M. Fareez
Chandramathi Samudi
Shamala Devi Sekaran
Mahendran Sekar
Rhanye Mac Guad
author_facet Nur Syafiqah Rahim
Yuan Seng Wu
Maw Shin Sim
Appalaraju Velaga
Srinivasa Reddy Bonam
Subash C. B. Gopinath
Vetriselvan Subramaniyan
Ker Woon Choy
Sin-Yeang Teow
Ismail M. Fareez
Chandramathi Samudi
Shamala Devi Sekaran
Mahendran Sekar
Rhanye Mac Guad
author_sort Nur Syafiqah Rahim
collection UMS
description There are six members of the transmembrane 4 superfamily (TM4SF) that have similar topology and sequence homology. Physiologically, they regulate tissue differentiation, signal transduction pathways, cellular activation, proliferation, motility, adhesion, and angiogenesis. Accumulating evidence has demonstrated, among six TM4SF members, the regulatory roles of transmembrane 4 L6 domain family members, particularly TM4SF1, TM4SF4, and TM4SF5, in cancer angiogenesis, progression, and chemoresistance. Hence, targeting derailed TM4SF for cancer therapy has become an emerging research area. As compared to others, this review aimed to present a focused insight and update on the biological roles of TM4SF1, TM4SF4, and TM4SF5 in the progression, metastasis, and chemoresistance of various cancers. Additionally, the mechanistic pathways, diagnostic and prognostic values, and the potential and efficacy of current anti-TM4SF antibody treatment were also deciphered. It also recommended the exploration of other interactive molecules to be implicated in cancer progression and chemoresistance, as well as potential therapeutic agents targeting TM4SF as future perspectives. Generally, these three TM4SF members interact with different integrins andreceptors to significantly induce intracellular signaling and regulate the proliferation, migration, and invasion of cancer cells. Intriguingly, gene silencing or anti-TM4SF antibody could reverse their regulatory roles deciphered in different preclinical models. They also have prognostic and diagnostic value as their high expression was detected in clinical tissues and cells of various cancers. Hence, TM4SF1, TM4SF4, and TM4SF5 are promising therapeutic targets for different cancer types preclinically and deserve further investigation.
first_indexed 2024-03-06T03:23:58Z
format Article
id ums.eprints-35751
institution Universiti Malaysia Sabah
language English
English
last_indexed 2024-03-06T03:23:58Z
publishDate 2023
publisher Molecular Diversity Preservation International (MDPI)
record_format dspace
spelling ums.eprints-357512023-06-30T01:35:31Z https://eprints.ums.edu.my/id/eprint/35751/ Three members of transmembrane-4-superfamily, tm4sf1, Tm4sf4, and tm4sf5, as emerging anticancer molecular Targets against cancer phenotypes and chemoresistance Nur Syafiqah Rahim Yuan Seng Wu Maw Shin Sim Appalaraju Velaga Srinivasa Reddy Bonam Subash C. B. Gopinath Vetriselvan Subramaniyan Ker Woon Choy Sin-Yeang Teow Ismail M. Fareez Chandramathi Samudi Shamala Devi Sekaran Mahendran Sekar Rhanye Mac Guad QP501-801 Animal biochemistry RC254-282 Neoplasms. Tumors. Oncology Including cancer and carcinogens There are six members of the transmembrane 4 superfamily (TM4SF) that have similar topology and sequence homology. Physiologically, they regulate tissue differentiation, signal transduction pathways, cellular activation, proliferation, motility, adhesion, and angiogenesis. Accumulating evidence has demonstrated, among six TM4SF members, the regulatory roles of transmembrane 4 L6 domain family members, particularly TM4SF1, TM4SF4, and TM4SF5, in cancer angiogenesis, progression, and chemoresistance. Hence, targeting derailed TM4SF for cancer therapy has become an emerging research area. As compared to others, this review aimed to present a focused insight and update on the biological roles of TM4SF1, TM4SF4, and TM4SF5 in the progression, metastasis, and chemoresistance of various cancers. Additionally, the mechanistic pathways, diagnostic and prognostic values, and the potential and efficacy of current anti-TM4SF antibody treatment were also deciphered. It also recommended the exploration of other interactive molecules to be implicated in cancer progression and chemoresistance, as well as potential therapeutic agents targeting TM4SF as future perspectives. Generally, these three TM4SF members interact with different integrins andreceptors to significantly induce intracellular signaling and regulate the proliferation, migration, and invasion of cancer cells. Intriguingly, gene silencing or anti-TM4SF antibody could reverse their regulatory roles deciphered in different preclinical models. They also have prognostic and diagnostic value as their high expression was detected in clinical tissues and cells of various cancers. Hence, TM4SF1, TM4SF4, and TM4SF5 are promising therapeutic targets for different cancer types preclinically and deserve further investigation. Molecular Diversity Preservation International (MDPI) 2023 Article NonPeerReviewed text en https://eprints.ums.edu.my/id/eprint/35751/1/ABSTRACT.pdf text en https://eprints.ums.edu.my/id/eprint/35751/2/FULL%20%20TEXT.pdf Nur Syafiqah Rahim and Yuan Seng Wu and Maw Shin Sim and Appalaraju Velaga and Srinivasa Reddy Bonam and Subash C. B. Gopinath and Vetriselvan Subramaniyan and Ker Woon Choy and Sin-Yeang Teow and Ismail M. Fareez and Chandramathi Samudi and Shamala Devi Sekaran and Mahendran Sekar and Rhanye Mac Guad (2023) Three members of transmembrane-4-superfamily, tm4sf1, Tm4sf4, and tm4sf5, as emerging anticancer molecular Targets against cancer phenotypes and chemoresistance. Pharmaceuticals, 16. pp. 1-27. https://doi.org/10.3390/ph16010110
spellingShingle QP501-801 Animal biochemistry
RC254-282 Neoplasms. Tumors. Oncology Including cancer and carcinogens
Nur Syafiqah Rahim
Yuan Seng Wu
Maw Shin Sim
Appalaraju Velaga
Srinivasa Reddy Bonam
Subash C. B. Gopinath
Vetriselvan Subramaniyan
Ker Woon Choy
Sin-Yeang Teow
Ismail M. Fareez
Chandramathi Samudi
Shamala Devi Sekaran
Mahendran Sekar
Rhanye Mac Guad
Three members of transmembrane-4-superfamily, tm4sf1, Tm4sf4, and tm4sf5, as emerging anticancer molecular Targets against cancer phenotypes and chemoresistance
title Three members of transmembrane-4-superfamily, tm4sf1, Tm4sf4, and tm4sf5, as emerging anticancer molecular Targets against cancer phenotypes and chemoresistance
title_full Three members of transmembrane-4-superfamily, tm4sf1, Tm4sf4, and tm4sf5, as emerging anticancer molecular Targets against cancer phenotypes and chemoresistance
title_fullStr Three members of transmembrane-4-superfamily, tm4sf1, Tm4sf4, and tm4sf5, as emerging anticancer molecular Targets against cancer phenotypes and chemoresistance
title_full_unstemmed Three members of transmembrane-4-superfamily, tm4sf1, Tm4sf4, and tm4sf5, as emerging anticancer molecular Targets against cancer phenotypes and chemoresistance
title_short Three members of transmembrane-4-superfamily, tm4sf1, Tm4sf4, and tm4sf5, as emerging anticancer molecular Targets against cancer phenotypes and chemoresistance
title_sort three members of transmembrane 4 superfamily tm4sf1 tm4sf4 and tm4sf5 as emerging anticancer molecular targets against cancer phenotypes and chemoresistance
topic QP501-801 Animal biochemistry
RC254-282 Neoplasms. Tumors. Oncology Including cancer and carcinogens
url https://eprints.ums.edu.my/id/eprint/35751/1/ABSTRACT.pdf
https://eprints.ums.edu.my/id/eprint/35751/2/FULL%20%20TEXT.pdf
work_keys_str_mv AT nursyafiqahrahim threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT yuansengwu threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT mawshinsim threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT appalarajuvelaga threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT srinivasareddybonam threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT subashcbgopinath threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT vetriselvansubramaniyan threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT kerwoonchoy threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT sinyeangteow threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT ismailmfareez threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT chandramathisamudi threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT shamaladevisekaran threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT mahendransekar threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance
AT rhanyemacguad threemembersoftransmembrane4superfamilytm4sf1tm4sf4andtm4sf5asemerginganticancermoleculartargetsagainstcancerphenotypesandchemoresistance