Loading…
New trends in glioma cancer therapy: Targeting Na+/H + exchangers
Glioma is the oneof the most prevalent primarybrain tumors. There is a variety of oxidative stresses, inflammatory pathways, apoptosis signaling, and Na+/H + exchangers (NHEs) involved in the pathophysiology of glioma. Previous studies have indicated a relationship between NHEs and some molecular pa...
Saved in:
Published in: | Journal of cellular physiology 2020-02, Vol.235 (2), p.658-665 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3534-7eb7ec7566565fc7c8765995cdde92c9c2dbd16606665a942a6d918e53ba32f83 |
---|---|
cites | cdi_FETCH-LOGICAL-c3534-7eb7ec7566565fc7c8765995cdde92c9c2dbd16606665a942a6d918e53ba32f83 |
container_end_page | 665 |
container_issue | 2 |
container_start_page | 658 |
container_title | Journal of cellular physiology |
container_volume | 235 |
creator | Tamtaji, Omid Reza Mirzaei, Hamed Shamshirian, Amir Shamshirian, Danial Behnam, Mohammad Asemi, Zatollah |
description | Glioma is the oneof the most prevalent primarybrain tumors. There is a variety of oxidative stresses, inflammatory pathways, apoptosis signaling, and Na+/H
+ exchangers (NHEs) involved in the pathophysiology of glioma. Previous studies have indicated a relationship between NHEs and some molecular pathways in glioma. NHEs, including NHE1, NHE5, and NHE9 affect apoptosis, tumor‐associated macrophage inflammatory pathways, matrix metalloproteinases, cancer‐cell growth, invasion, and migration of glioma. Also, inhibition of NHEs contributes to increased survival in animal models of glioma. Limited studies, however, have assessed the relationship between NHEs and molecular pathways in glioma. This review summarizes current knowledge and evidence regarding the relationship between NHEs and glioma, and the mechanisms involved.
Previous studies have indicated a relationship between Na+/H
+ exchangers (NHEs) and some molecular pathways in glioma. NHEs, including NHE1, NHE5, and NHE9 affect apoptosis, tumor‐associated macrophage inflammatory pathways, matrix metalloproteinases, cancer‐cell growth, invasion, and migration of glioma. Also, inhibition of NHEs contributes to increased survival in the animal models of glioma. |
doi_str_mv | 10.1002/jcp.29014 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2250638101</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2317568682</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3534-7eb7ec7566565fc7c8765995cdde92c9c2dbd16606665a942a6d918e53ba32f83</originalsourceid><addsrcrecordid>eNp10E1PAjEQBuDGaATRg3_ANPGiIQv92Ha33ghR0RD0gOem2x1gybKL7RLk31sFPZh4msM8eTPzInRJSY8SwvpLu-4xRWh8hNqUqCSKpWDHqB12NFIipi105v2SEKIU56eoxSkTJI7jNhpMYIsbB1XucVHheVnUK4OtqSw43CzAmfXuDk-Nm0NTVHM8Md3-CHcxfNiFqebg_Dk6mZnSw8VhdtDbw_10OIrGL49Pw8E4slzwOEogS8AmQkohxcwmNk2kUErYPAfFrLIsz3IqJZFBGBUzI3NFUxA8M5zNUt5BN_vctavfN-AbvSq8hbI0FdQbr1l4SfKUEhro9R-6rDeuCtdpxmm4IZUpC-p2r6yrvXcw02tXrIzbaUr0V6869Kq_ew326pC4yVaQ_8qfIgPo78G2KGH3f5J-Hr7uIz8BZLB-Yg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2317568682</pqid></control><display><type>article</type><title>New trends in glioma cancer therapy: Targeting Na+/H + exchangers</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Tamtaji, Omid Reza ; Mirzaei, Hamed ; Shamshirian, Amir ; Shamshirian, Danial ; Behnam, Mohammad ; Asemi, Zatollah</creator><creatorcontrib>Tamtaji, Omid Reza ; Mirzaei, Hamed ; Shamshirian, Amir ; Shamshirian, Danial ; Behnam, Mohammad ; Asemi, Zatollah</creatorcontrib><description>Glioma is the oneof the most prevalent primarybrain tumors. There is a variety of oxidative stresses, inflammatory pathways, apoptosis signaling, and Na+/H
+ exchangers (NHEs) involved in the pathophysiology of glioma. Previous studies have indicated a relationship between NHEs and some molecular pathways in glioma. NHEs, including NHE1, NHE5, and NHE9 affect apoptosis, tumor‐associated macrophage inflammatory pathways, matrix metalloproteinases, cancer‐cell growth, invasion, and migration of glioma. Also, inhibition of NHEs contributes to increased survival in animal models of glioma. Limited studies, however, have assessed the relationship between NHEs and molecular pathways in glioma. This review summarizes current knowledge and evidence regarding the relationship between NHEs and glioma, and the mechanisms involved.
Previous studies have indicated a relationship between Na+/H
+ exchangers (NHEs) and some molecular pathways in glioma. NHEs, including NHE1, NHE5, and NHE9 affect apoptosis, tumor‐associated macrophage inflammatory pathways, matrix metalloproteinases, cancer‐cell growth, invasion, and migration of glioma. Also, inhibition of NHEs contributes to increased survival in the animal models of glioma.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.29014</identifier><identifier>PMID: 31250444</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Animal models ; Apoptosis ; Brain tumors ; Cancer ; Cancer therapies ; Glioma ; Hydrogen ; Inflammation ; Leukocyte migration ; Macrophages ; Matrix metalloproteinase ; Matrix metalloproteinases ; Na+/H + exchangers ; Na+/H+-exchanging ATPase ; Oxidative stress ; Tumors</subject><ispartof>Journal of cellular physiology, 2020-02, Vol.235 (2), p.658-665</ispartof><rights>2019 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3534-7eb7ec7566565fc7c8765995cdde92c9c2dbd16606665a942a6d918e53ba32f83</citedby><cites>FETCH-LOGICAL-c3534-7eb7ec7566565fc7c8765995cdde92c9c2dbd16606665a942a6d918e53ba32f83</cites><orcidid>0000-0003-2492-3996 ; 0000-0001-5265-4792 ; 0000-0002-9399-8281</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31250444$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tamtaji, Omid Reza</creatorcontrib><creatorcontrib>Mirzaei, Hamed</creatorcontrib><creatorcontrib>Shamshirian, Amir</creatorcontrib><creatorcontrib>Shamshirian, Danial</creatorcontrib><creatorcontrib>Behnam, Mohammad</creatorcontrib><creatorcontrib>Asemi, Zatollah</creatorcontrib><title>New trends in glioma cancer therapy: Targeting Na+/H + exchangers</title><title>Journal of cellular physiology</title><addtitle>J Cell Physiol</addtitle><description>Glioma is the oneof the most prevalent primarybrain tumors. There is a variety of oxidative stresses, inflammatory pathways, apoptosis signaling, and Na+/H
+ exchangers (NHEs) involved in the pathophysiology of glioma. Previous studies have indicated a relationship between NHEs and some molecular pathways in glioma. NHEs, including NHE1, NHE5, and NHE9 affect apoptosis, tumor‐associated macrophage inflammatory pathways, matrix metalloproteinases, cancer‐cell growth, invasion, and migration of glioma. Also, inhibition of NHEs contributes to increased survival in animal models of glioma. Limited studies, however, have assessed the relationship between NHEs and molecular pathways in glioma. This review summarizes current knowledge and evidence regarding the relationship between NHEs and glioma, and the mechanisms involved.
Previous studies have indicated a relationship between Na+/H
+ exchangers (NHEs) and some molecular pathways in glioma. NHEs, including NHE1, NHE5, and NHE9 affect apoptosis, tumor‐associated macrophage inflammatory pathways, matrix metalloproteinases, cancer‐cell growth, invasion, and migration of glioma. Also, inhibition of NHEs contributes to increased survival in the animal models of glioma.</description><subject>Animal models</subject><subject>Apoptosis</subject><subject>Brain tumors</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Glioma</subject><subject>Hydrogen</subject><subject>Inflammation</subject><subject>Leukocyte migration</subject><subject>Macrophages</subject><subject>Matrix metalloproteinase</subject><subject>Matrix metalloproteinases</subject><subject>Na+/H + exchangers</subject><subject>Na+/H+-exchanging ATPase</subject><subject>Oxidative stress</subject><subject>Tumors</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp10E1PAjEQBuDGaATRg3_ANPGiIQv92Ha33ghR0RD0gOem2x1gybKL7RLk31sFPZh4msM8eTPzInRJSY8SwvpLu-4xRWh8hNqUqCSKpWDHqB12NFIipi105v2SEKIU56eoxSkTJI7jNhpMYIsbB1XucVHheVnUK4OtqSw43CzAmfXuDk-Nm0NTVHM8Md3-CHcxfNiFqebg_Dk6mZnSw8VhdtDbw_10OIrGL49Pw8E4slzwOEogS8AmQkohxcwmNk2kUErYPAfFrLIsz3IqJZFBGBUzI3NFUxA8M5zNUt5BN_vctavfN-AbvSq8hbI0FdQbr1l4SfKUEhro9R-6rDeuCtdpxmm4IZUpC-p2r6yrvXcw02tXrIzbaUr0V6869Kq_ew326pC4yVaQ_8qfIgPo78G2KGH3f5J-Hr7uIz8BZLB-Yg</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Tamtaji, Omid Reza</creator><creator>Mirzaei, Hamed</creator><creator>Shamshirian, Amir</creator><creator>Shamshirian, Danial</creator><creator>Behnam, Mohammad</creator><creator>Asemi, Zatollah</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2492-3996</orcidid><orcidid>https://orcid.org/0000-0001-5265-4792</orcidid><orcidid>https://orcid.org/0000-0002-9399-8281</orcidid></search><sort><creationdate>202002</creationdate><title>New trends in glioma cancer therapy: Targeting Na+/H + exchangers</title><author>Tamtaji, Omid Reza ; Mirzaei, Hamed ; Shamshirian, Amir ; Shamshirian, Danial ; Behnam, Mohammad ; Asemi, Zatollah</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3534-7eb7ec7566565fc7c8765995cdde92c9c2dbd16606665a942a6d918e53ba32f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animal models</topic><topic>Apoptosis</topic><topic>Brain tumors</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Glioma</topic><topic>Hydrogen</topic><topic>Inflammation</topic><topic>Leukocyte migration</topic><topic>Macrophages</topic><topic>Matrix metalloproteinase</topic><topic>Matrix metalloproteinases</topic><topic>Na+/H + exchangers</topic><topic>Na+/H+-exchanging ATPase</topic><topic>Oxidative stress</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tamtaji, Omid Reza</creatorcontrib><creatorcontrib>Mirzaei, Hamed</creatorcontrib><creatorcontrib>Shamshirian, Amir</creatorcontrib><creatorcontrib>Shamshirian, Danial</creatorcontrib><creatorcontrib>Behnam, Mohammad</creatorcontrib><creatorcontrib>Asemi, Zatollah</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tamtaji, Omid Reza</au><au>Mirzaei, Hamed</au><au>Shamshirian, Amir</au><au>Shamshirian, Danial</au><au>Behnam, Mohammad</au><au>Asemi, Zatollah</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New trends in glioma cancer therapy: Targeting Na+/H + exchangers</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J Cell Physiol</addtitle><date>2020-02</date><risdate>2020</risdate><volume>235</volume><issue>2</issue><spage>658</spage><epage>665</epage><pages>658-665</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>Glioma is the oneof the most prevalent primarybrain tumors. There is a variety of oxidative stresses, inflammatory pathways, apoptosis signaling, and Na+/H
+ exchangers (NHEs) involved in the pathophysiology of glioma. Previous studies have indicated a relationship between NHEs and some molecular pathways in glioma. NHEs, including NHE1, NHE5, and NHE9 affect apoptosis, tumor‐associated macrophage inflammatory pathways, matrix metalloproteinases, cancer‐cell growth, invasion, and migration of glioma. Also, inhibition of NHEs contributes to increased survival in animal models of glioma. Limited studies, however, have assessed the relationship between NHEs and molecular pathways in glioma. This review summarizes current knowledge and evidence regarding the relationship between NHEs and glioma, and the mechanisms involved.
Previous studies have indicated a relationship between Na+/H
+ exchangers (NHEs) and some molecular pathways in glioma. NHEs, including NHE1, NHE5, and NHE9 affect apoptosis, tumor‐associated macrophage inflammatory pathways, matrix metalloproteinases, cancer‐cell growth, invasion, and migration of glioma. Also, inhibition of NHEs contributes to increased survival in the animal models of glioma.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31250444</pmid><doi>10.1002/jcp.29014</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-2492-3996</orcidid><orcidid>https://orcid.org/0000-0001-5265-4792</orcidid><orcidid>https://orcid.org/0000-0002-9399-8281</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9541 |
ispartof | Journal of cellular physiology, 2020-02, Vol.235 (2), p.658-665 |
issn | 0021-9541 1097-4652 |
language | eng |
recordid | cdi_proquest_miscellaneous_2250638101 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Animal models Apoptosis Brain tumors Cancer Cancer therapies Glioma Hydrogen Inflammation Leukocyte migration Macrophages Matrix metalloproteinase Matrix metalloproteinases Na+/H + exchangers Na+/H+-exchanging ATPase Oxidative stress Tumors |
title | New trends in glioma cancer therapy: Targeting Na+/H + exchangers |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T04%3A26%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=New%20trends%20in%20glioma%20cancer%20therapy:%20Targeting%20Na+/H%20+%20exchangers&rft.jtitle=Journal%20of%20cellular%20physiology&rft.au=Tamtaji,%20Omid%20Reza&rft.date=2020-02&rft.volume=235&rft.issue=2&rft.spage=658&rft.epage=665&rft.pages=658-665&rft.issn=0021-9541&rft.eissn=1097-4652&rft_id=info:doi/10.1002/jcp.29014&rft_dat=%3Cproquest_cross%3E2317568682%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3534-7eb7ec7566565fc7c8765995cdde92c9c2dbd16606665a942a6d918e53ba32f83%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2317568682&rft_id=info:pmid/31250444&rfr_iscdi=true |