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  1. Article ; Online: Targeted silencing of TRPM7 ion channel induces replicative senescence and produces enhanced cytotoxicity with gemcitabine in pancreatic adenocarcinoma.

    Yee, Nelson S / Zhou, Weiqiang / Lee, Minsun / Yee, Rosemary K

    Cancer letters

    2011  Volume 318, Issue 1, Page(s) 99–105

    Abstract: ... cytotoxicity as compared to gemcitabine alone. Thus, TRPM7 is required for preventing senescence, and ... regulation of p16(CDKN2A) and WRN mRNA. The combination of anti-TRPM7 siRNA and gemcitabine produced enhanced ... in pancreatic epithelia and adenocarcinoma. To elucidate the mechanism that mediates the function of TRPM7 ...

    Abstract The transient receptor potential TRPM7 ion channel is required for cellular proliferation in pancreatic epithelia and adenocarcinoma. To elucidate the mechanism that mediates the function of TRPM7, we examined its role in survival of pancreatic cancer cells. RNA interference-mediated silencing of TRPM7 did not induce apoptotic cell death. TRPM7-deficient cells underwent replicative senescence with up-regulation of p16(CDKN2A) and WRN mRNA. The combination of anti-TRPM7 siRNA and gemcitabine produced enhanced cytotoxicity as compared to gemcitabine alone. Thus, TRPM7 is required for preventing senescence, and modulation of TRPM7 expression may help improve treatment response of pancreatic cancer by combining with apoptosis-inducing agents.
    MeSH term(s) Adenocarcinoma/drug therapy ; Adenocarcinoma/metabolism ; Adenocarcinoma/pathology ; Antimetabolites, Antineoplastic/pharmacology ; Apoptosis ; Blotting, Western ; Cell Line, Tumor ; Cell Proliferation ; Cellular Senescence ; Cyclin-Dependent Kinase Inhibitor p16/genetics ; Cyclin-Dependent Kinase Inhibitor p16/metabolism ; Cyclin-Dependent Kinase Inhibitor p27/genetics ; Cyclin-Dependent Kinase Inhibitor p27/metabolism ; Deoxycytidine/analogs & derivatives ; Deoxycytidine/pharmacology ; Exodeoxyribonucleases/genetics ; Exodeoxyribonucleases/metabolism ; Humans ; Pancreatic Neoplasms/drug therapy ; Pancreatic Neoplasms/metabolism ; Pancreatic Neoplasms/pathology ; RNA Interference ; RNA, Messenger/genetics ; RNA, Small Interfering/genetics ; Real-Time Polymerase Chain Reaction ; RecQ Helicases/genetics ; RecQ Helicases/metabolism ; Werner Syndrome Helicase
    Chemical Substances Antimetabolites, Antineoplastic ; CDKN1B protein, human ; Cyclin-Dependent Kinase Inhibitor p16 ; RNA, Messenger ; RNA, Small Interfering ; Deoxycytidine (0W860991D6) ; Cyclin-Dependent Kinase Inhibitor p27 (147604-94-2) ; gemcitabine (B76N6SBZ8R) ; Exodeoxyribonucleases (EC 3.1.-) ; RecQ Helicases (EC 3.6.4.12) ; WRN protein, human (EC 3.6.4.12) ; Werner Syndrome Helicase (EC 3.6.4.12)
    Language English
    Publishing date 2011-12-11
    Publishing country Ireland
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 195674-7
    ISSN 1872-7980 ; 0304-3835
    ISSN (online) 1872-7980
    ISSN 0304-3835
    DOI 10.1016/j.canlet.2011.12.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Targeted silencing of TRPM7 ion channel induces replicative senescence and produces enhanced cytotoxicity with gemcitabine in pancreatic adenocarcinoma

    Yee, Nelson S / Zhou, Weiqiang / Lee, Minsun / Yee, Rosemary K

    Cancer letters. 2012 May 1, v. 318, no. 1

    2012  

    Abstract: ... cytotoxicity as compared to gemcitabine alone. Thus, TRPM7 is required for preventing senescence, and ... regulation of p16Cᴰᴷᴺ²ᴬ and WRN mRNA. The combination of anti-TRPM7 siRNA and gemcitabine produced enhanced ... in pancreatic epithelia and adenocarcinoma. To elucidate the mechanism that mediates the function of TRPM7 ...

    Abstract The transient receptor potential TRPM7 ion channel is required for cellular proliferation in pancreatic epithelia and adenocarcinoma. To elucidate the mechanism that mediates the function of TRPM7, we examined its role in survival of pancreatic cancer cells. RNA interference-mediated silencing of TRPM7 did not induce apoptotic cell death. TRPM7-deficient cells underwent replicative senescence with up-regulation of p16Cᴰᴷᴺ²ᴬ and WRN mRNA. The combination of anti-TRPM7 siRNA and gemcitabine produced enhanced cytotoxicity as compared to gemcitabine alone. Thus, TRPM7 is required for preventing senescence, and modulation of TRPM7 expression may help improve treatment response of pancreatic cancer by combining with apoptosis-inducing agents.
    Keywords RNA ; adenocarcinoma ; apoptosis ; cell proliferation ; cytotoxicity ; gene expression regulation ; ion channels ; pancreatic neoplasms ; senescence
    Language English
    Dates of publication 2012-0501
    Size p. 99-105.
    Publishing place Elsevier Ireland Ltd
    Document type Article
    ZDB-ID 195674-7
    ISSN 1872-7980 ; 0304-3835
    ISSN (online) 1872-7980
    ISSN 0304-3835
    DOI 10.1016/j.canlet.2011.12.007
    Database NAL-Catalogue (AGRICOLA)

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  3. Article: Targeted silencing of TRPM7 ion channel induces replicative senescence and produces enhanced cytotoxicity with gemcitabine in pancreatic adenocarcinoma

    Yee, Nelson S. / Zhou, Weiqiang / Lee, Minsun / Yee, Rosemary K.

    Cancer letters

    Volume v. 318,, Issue no. 1

    Abstract: ... cytotoxicity as compared to gemcitabine alone. Thus, TRPM7 is required for preventing senescence, and ... regulation of p16Cᴰᴷᴺ²ᴬ and WRN mRNA. The combination of anti-TRPM7 siRNA and gemcitabine produced enhanced ... in pancreatic epithelia and adenocarcinoma. To elucidate the mechanism that mediates the function of TRPM7 ...

    Abstract The transient receptor potential TRPM7 ion channel is required for cellular proliferation in pancreatic epithelia and adenocarcinoma. To elucidate the mechanism that mediates the function of TRPM7, we examined its role in survival of pancreatic cancer cells. RNA interference-mediated silencing of TRPM7 did not induce apoptotic cell death. TRPM7-deficient cells underwent replicative senescence with up-regulation of p16Cᴰᴷᴺ²ᴬ and WRN mRNA. The combination of anti-TRPM7 siRNA and gemcitabine produced enhanced cytotoxicity as compared to gemcitabine alone. Thus, TRPM7 is required for preventing senescence, and modulation of TRPM7 expression may help improve treatment response of pancreatic cancer by combining with apoptosis-inducing agents.
    Keywords cell proliferation ; ion channels ; RNA ; apoptosis ; adenocarcinoma ; senescence ; cytotoxicity ; pancreatic neoplasms ; gene expression regulation
    Language English
    Document type Article
    ISSN 0304-3835
    Database AGRIS - International Information System for the Agricultural Sciences and Technology

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