Loading…
HPIP is upregulated in colorectal cancer and regulates colorectal cancer cell proliferation, apoptosis and invasion
Hematopoietic pre-B cell leukemia transcription factor (PBX)-interacting protein (HPIP) was shown to play a role in cancer development and progression. However, the role of HPIP in colorectal cancer (CRC) is unknown. Here, we report that HPIP is overexpressed in most of CRC patients and predicts poo...
Saved in:
Published in: | Scientific reports 2015-03, Vol.5 (1), p.9429-9429, Article 9429 |
---|---|
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-c504t-e75021071f2ab3b71ff64e2412bc88e83ed4e29f25077c97b5ee261b95246e3c3 |
---|---|
cites | cdi_FETCH-LOGICAL-c504t-e75021071f2ab3b71ff64e2412bc88e83ed4e29f25077c97b5ee261b95246e3c3 |
container_end_page | 9429 |
container_issue | 1 |
container_start_page | 9429 |
container_title | Scientific reports |
container_volume | 5 |
creator | Feng, Yingying Xu, Xiaojie Zhang, Yunjing Ding, Jianhua Wang, Yonggang Zhang, Xiaopeng Wu, Zhe Kang, Lei Liang, Yingchun Zhou, LiYing Song, Santai Zhao, Ke Ye, Qinong |
description | Hematopoietic pre-B cell leukemia transcription factor (PBX)-interacting protein (HPIP) was shown to play a role in cancer development and progression. However, the role of HPIP in colorectal cancer (CRC) is unknown. Here, we report that HPIP is overexpressed in most of CRC patients and predicts poor clinical outcome in CRC. HPIP promotes CRC cell proliferation via activation of G1/S and G2/M checkpoint transitions, concomitant with a marked increase of the positive cell cycle regulators, including cyclin D1, cyclin A and cyclin B1. HPIP inhibits CRC cell apoptosis accompanied by the decreased levels of BAX and PIG3, the inducers of apoptosis and the increased level of the apoptosis inhibitor BCL2. HPIP blocks caspase-3-mediated cleavage of PARP, an important apoptosis marker. HPIP promotes CRC cell migration and invasion and regulates epithelial-mesenchymal transition (EMT), which plays a critical role in cancer cell migration and invasion. Activation of MAPK/ERK1/2 and PI3k/AKT pathways is required for HPIP modulation of CRC cell proliferation, migration and EMT. Moreover, HPIP knockdown suppresses colorectal tumor growth in nude mice. These data highlight the important role of HPIP in CRC cell proliferation and progression and suggest that HPIP may be a useful target for CRC therapy. |
doi_str_mv | 10.1038/srep09429 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4371107</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1666723515</sourcerecordid><originalsourceid>FETCH-LOGICAL-c504t-e75021071f2ab3b71ff64e2412bc88e83ed4e29f25077c97b5ee261b95246e3c3</originalsourceid><addsrcrecordid>eNptkU1PGzEQhq2qCFDgwB-oLPVSKgL-XK8vlVDUAhISHOBseZ3Z1NHG3tq7SP33dRQSpYAvY3ueeWdGL0JnlFxSwuurnKAnWjD9CR0zIuSUccY-792P0GnOS1KOZFpQfYiOmKwJUZofo3z7ePeIfcZjn2AxdnaAOfYBu9jFBG6wHXY2OEjYhjneIvmDvIOuw32KnW8h2cHHcIFtH_sh5iK_rvbhxebyf4IOWttlOH2NE_T86-fT7HZ6_3BzN7u-nzpJxDAFJQmjRNGW2YY3JbaVACYoa1xdQ81hXp66ZZIo5bRqJACraKMlExVwxyfox0a3H5sVzB2EIdnO9MmvbPprovXm_0zwv80ivhjBFS2Ni8C3V4EU_4yQB7Pyeb2nDRDHbGhVVYpxSWVBv75Bl3FMoaxnaK3rigup1oLnG8qlmItx7W4YSszaTbNzs7Bf9qffkVvvCvB9A-SSCgtIey3fqf0DF-Kquw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1898634577</pqid></control><display><type>article</type><title>HPIP is upregulated in colorectal cancer and regulates colorectal cancer cell proliferation, apoptosis and invasion</title><source>Publicly Available Content Database</source><source>Full-Text Journals in Chemistry (Open access)</source><source>PubMed</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Feng, Yingying ; Xu, Xiaojie ; Zhang, Yunjing ; Ding, Jianhua ; Wang, Yonggang ; Zhang, Xiaopeng ; Wu, Zhe ; Kang, Lei ; Liang, Yingchun ; Zhou, LiYing ; Song, Santai ; Zhao, Ke ; Ye, Qinong</creator><creatorcontrib>Feng, Yingying ; Xu, Xiaojie ; Zhang, Yunjing ; Ding, Jianhua ; Wang, Yonggang ; Zhang, Xiaopeng ; Wu, Zhe ; Kang, Lei ; Liang, Yingchun ; Zhou, LiYing ; Song, Santai ; Zhao, Ke ; Ye, Qinong</creatorcontrib><description>Hematopoietic pre-B cell leukemia transcription factor (PBX)-interacting protein (HPIP) was shown to play a role in cancer development and progression. However, the role of HPIP in colorectal cancer (CRC) is unknown. Here, we report that HPIP is overexpressed in most of CRC patients and predicts poor clinical outcome in CRC. HPIP promotes CRC cell proliferation via activation of G1/S and G2/M checkpoint transitions, concomitant with a marked increase of the positive cell cycle regulators, including cyclin D1, cyclin A and cyclin B1. HPIP inhibits CRC cell apoptosis accompanied by the decreased levels of BAX and PIG3, the inducers of apoptosis and the increased level of the apoptosis inhibitor BCL2. HPIP blocks caspase-3-mediated cleavage of PARP, an important apoptosis marker. HPIP promotes CRC cell migration and invasion and regulates epithelial-mesenchymal transition (EMT), which plays a critical role in cancer cell migration and invasion. Activation of MAPK/ERK1/2 and PI3k/AKT pathways is required for HPIP modulation of CRC cell proliferation, migration and EMT. Moreover, HPIP knockdown suppresses colorectal tumor growth in nude mice. These data highlight the important role of HPIP in CRC cell proliferation and progression and suggest that HPIP may be a useful target for CRC therapy.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep09429</identifier><identifier>PMID: 25800793</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>1-Phosphatidylinositol 3-kinase ; 13/109 ; 13/2 ; 13/31 ; 13/51 ; 13/89 ; 38/88 ; 45/44 ; 631/67/1504 ; 631/67/395 ; 64/60 ; 82/1 ; 82/80 ; 96/106 ; AKT protein ; Animals ; Apoptosis ; Apoptosis - genetics ; BAX protein ; Caspase ; Caspase-3 ; Cell activation ; Cell adhesion & migration ; Cell cycle ; Cell Cycle - genetics ; Cell Cycle Proteins - genetics ; Cell Cycle Proteins - metabolism ; Cell growth ; Cell Line, Tumor ; Cell migration ; Cell Movement - genetics ; Cell Proliferation ; Colorectal cancer ; Colorectal carcinoma ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - metabolism ; Colorectal Neoplasms - pathology ; Cyclin A ; Cyclin B1 ; Cyclin D1 ; Disease Models, Animal ; Epithelial-Mesenchymal Transition ; Gene Expression ; Gene Knockdown Techniques ; Heterografts ; Humanities and Social Sciences ; Humans ; Intracellular Signaling Peptides and Proteins - genetics ; Intracellular Signaling Peptides and Proteins - metabolism ; Leukemia ; Lymphocytes B ; MAP kinase ; Mesenchyme ; Mice ; Mitogen-Activated Protein Kinases - metabolism ; multidisciplinary ; Poly(ADP-ribose) polymerase ; Proto-Oncogene Proteins c-akt - metabolism ; Science ; Up-Regulation</subject><ispartof>Scientific reports, 2015-03, Vol.5 (1), p.9429-9429, Article 9429</ispartof><rights>The Author(s) 2015</rights><rights>Copyright Nature Publishing Group Mar 2015</rights><rights>Copyright © 2015, Macmillan Publishers Limited. All rights reserved 2015 Macmillan Publishers Limited. All rights reserved</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-e75021071f2ab3b71ff64e2412bc88e83ed4e29f25077c97b5ee261b95246e3c3</citedby><cites>FETCH-LOGICAL-c504t-e75021071f2ab3b71ff64e2412bc88e83ed4e29f25077c97b5ee261b95246e3c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1898634577/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1898634577?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25800793$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feng, Yingying</creatorcontrib><creatorcontrib>Xu, Xiaojie</creatorcontrib><creatorcontrib>Zhang, Yunjing</creatorcontrib><creatorcontrib>Ding, Jianhua</creatorcontrib><creatorcontrib>Wang, Yonggang</creatorcontrib><creatorcontrib>Zhang, Xiaopeng</creatorcontrib><creatorcontrib>Wu, Zhe</creatorcontrib><creatorcontrib>Kang, Lei</creatorcontrib><creatorcontrib>Liang, Yingchun</creatorcontrib><creatorcontrib>Zhou, LiYing</creatorcontrib><creatorcontrib>Song, Santai</creatorcontrib><creatorcontrib>Zhao, Ke</creatorcontrib><creatorcontrib>Ye, Qinong</creatorcontrib><title>HPIP is upregulated in colorectal cancer and regulates colorectal cancer cell proliferation, apoptosis and invasion</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Hematopoietic pre-B cell leukemia transcription factor (PBX)-interacting protein (HPIP) was shown to play a role in cancer development and progression. However, the role of HPIP in colorectal cancer (CRC) is unknown. Here, we report that HPIP is overexpressed in most of CRC patients and predicts poor clinical outcome in CRC. HPIP promotes CRC cell proliferation via activation of G1/S and G2/M checkpoint transitions, concomitant with a marked increase of the positive cell cycle regulators, including cyclin D1, cyclin A and cyclin B1. HPIP inhibits CRC cell apoptosis accompanied by the decreased levels of BAX and PIG3, the inducers of apoptosis and the increased level of the apoptosis inhibitor BCL2. HPIP blocks caspase-3-mediated cleavage of PARP, an important apoptosis marker. HPIP promotes CRC cell migration and invasion and regulates epithelial-mesenchymal transition (EMT), which plays a critical role in cancer cell migration and invasion. Activation of MAPK/ERK1/2 and PI3k/AKT pathways is required for HPIP modulation of CRC cell proliferation, migration and EMT. Moreover, HPIP knockdown suppresses colorectal tumor growth in nude mice. These data highlight the important role of HPIP in CRC cell proliferation and progression and suggest that HPIP may be a useful target for CRC therapy.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>13/109</subject><subject>13/2</subject><subject>13/31</subject><subject>13/51</subject><subject>13/89</subject><subject>38/88</subject><subject>45/44</subject><subject>631/67/1504</subject><subject>631/67/395</subject><subject>64/60</subject><subject>82/1</subject><subject>82/80</subject><subject>96/106</subject><subject>AKT protein</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - genetics</subject><subject>BAX protein</subject><subject>Caspase</subject><subject>Caspase-3</subject><subject>Cell activation</subject><subject>Cell adhesion & migration</subject><subject>Cell cycle</subject><subject>Cell Cycle - genetics</subject><subject>Cell Cycle Proteins - genetics</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell migration</subject><subject>Cell Movement - genetics</subject><subject>Cell Proliferation</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Cyclin A</subject><subject>Cyclin B1</subject><subject>Cyclin D1</subject><subject>Disease Models, Animal</subject><subject>Epithelial-Mesenchymal Transition</subject><subject>Gene Expression</subject><subject>Gene Knockdown Techniques</subject><subject>Heterografts</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Leukemia</subject><subject>Lymphocytes B</subject><subject>MAP kinase</subject><subject>Mesenchyme</subject><subject>Mice</subject><subject>Mitogen-Activated Protein Kinases - metabolism</subject><subject>multidisciplinary</subject><subject>Poly(ADP-ribose) polymerase</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Science</subject><subject>Up-Regulation</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkU1PGzEQhq2qCFDgwB-oLPVSKgL-XK8vlVDUAhISHOBseZ3Z1NHG3tq7SP33dRQSpYAvY3ueeWdGL0JnlFxSwuurnKAnWjD9CR0zIuSUccY-792P0GnOS1KOZFpQfYiOmKwJUZofo3z7ePeIfcZjn2AxdnaAOfYBu9jFBG6wHXY2OEjYhjneIvmDvIOuw32KnW8h2cHHcIFtH_sh5iK_rvbhxebyf4IOWttlOH2NE_T86-fT7HZ6_3BzN7u-nzpJxDAFJQmjRNGW2YY3JbaVACYoa1xdQ81hXp66ZZIo5bRqJACraKMlExVwxyfox0a3H5sVzB2EIdnO9MmvbPprovXm_0zwv80ivhjBFS2Ni8C3V4EU_4yQB7Pyeb2nDRDHbGhVVYpxSWVBv75Bl3FMoaxnaK3rigup1oLnG8qlmItx7W4YSszaTbNzs7Bf9qffkVvvCvB9A-SSCgtIey3fqf0DF-Kquw</recordid><startdate>20150324</startdate><enddate>20150324</enddate><creator>Feng, Yingying</creator><creator>Xu, Xiaojie</creator><creator>Zhang, Yunjing</creator><creator>Ding, Jianhua</creator><creator>Wang, Yonggang</creator><creator>Zhang, Xiaopeng</creator><creator>Wu, Zhe</creator><creator>Kang, Lei</creator><creator>Liang, Yingchun</creator><creator>Zhou, LiYing</creator><creator>Song, Santai</creator><creator>Zhao, Ke</creator><creator>Ye, Qinong</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150324</creationdate><title>HPIP is upregulated in colorectal cancer and regulates colorectal cancer cell proliferation, apoptosis and invasion</title><author>Feng, Yingying ; Xu, Xiaojie ; Zhang, Yunjing ; Ding, Jianhua ; Wang, Yonggang ; Zhang, Xiaopeng ; Wu, Zhe ; Kang, Lei ; Liang, Yingchun ; Zhou, LiYing ; Song, Santai ; Zhao, Ke ; Ye, Qinong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c504t-e75021071f2ab3b71ff64e2412bc88e83ed4e29f25077c97b5ee261b95246e3c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>13/109</topic><topic>13/2</topic><topic>13/31</topic><topic>13/51</topic><topic>13/89</topic><topic>38/88</topic><topic>45/44</topic><topic>631/67/1504</topic><topic>631/67/395</topic><topic>64/60</topic><topic>82/1</topic><topic>82/80</topic><topic>96/106</topic><topic>AKT protein</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - genetics</topic><topic>BAX protein</topic><topic>Caspase</topic><topic>Caspase-3</topic><topic>Cell activation</topic><topic>Cell adhesion & migration</topic><topic>Cell cycle</topic><topic>Cell Cycle - genetics</topic><topic>Cell Cycle Proteins - genetics</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cell growth</topic><topic>Cell Line, Tumor</topic><topic>Cell migration</topic><topic>Cell Movement - genetics</topic><topic>Cell Proliferation</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Cyclin A</topic><topic>Cyclin B1</topic><topic>Cyclin D1</topic><topic>Disease Models, Animal</topic><topic>Epithelial-Mesenchymal Transition</topic><topic>Gene Expression</topic><topic>Gene Knockdown Techniques</topic><topic>Heterografts</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Intracellular Signaling Peptides and Proteins - genetics</topic><topic>Intracellular Signaling Peptides and Proteins - metabolism</topic><topic>Leukemia</topic><topic>Lymphocytes B</topic><topic>MAP kinase</topic><topic>Mesenchyme</topic><topic>Mice</topic><topic>Mitogen-Activated Protein Kinases - metabolism</topic><topic>multidisciplinary</topic><topic>Poly(ADP-ribose) polymerase</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>Science</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feng, Yingying</creatorcontrib><creatorcontrib>Xu, Xiaojie</creatorcontrib><creatorcontrib>Zhang, Yunjing</creatorcontrib><creatorcontrib>Ding, Jianhua</creatorcontrib><creatorcontrib>Wang, Yonggang</creatorcontrib><creatorcontrib>Zhang, Xiaopeng</creatorcontrib><creatorcontrib>Wu, Zhe</creatorcontrib><creatorcontrib>Kang, Lei</creatorcontrib><creatorcontrib>Liang, Yingchun</creatorcontrib><creatorcontrib>Zhou, LiYing</creatorcontrib><creatorcontrib>Song, Santai</creatorcontrib><creatorcontrib>Zhao, Ke</creatorcontrib><creatorcontrib>Ye, Qinong</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feng, Yingying</au><au>Xu, Xiaojie</au><au>Zhang, Yunjing</au><au>Ding, Jianhua</au><au>Wang, Yonggang</au><au>Zhang, Xiaopeng</au><au>Wu, Zhe</au><au>Kang, Lei</au><au>Liang, Yingchun</au><au>Zhou, LiYing</au><au>Song, Santai</au><au>Zhao, Ke</au><au>Ye, Qinong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HPIP is upregulated in colorectal cancer and regulates colorectal cancer cell proliferation, apoptosis and invasion</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2015-03-24</date><risdate>2015</risdate><volume>5</volume><issue>1</issue><spage>9429</spage><epage>9429</epage><pages>9429-9429</pages><artnum>9429</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Hematopoietic pre-B cell leukemia transcription factor (PBX)-interacting protein (HPIP) was shown to play a role in cancer development and progression. However, the role of HPIP in colorectal cancer (CRC) is unknown. Here, we report that HPIP is overexpressed in most of CRC patients and predicts poor clinical outcome in CRC. HPIP promotes CRC cell proliferation via activation of G1/S and G2/M checkpoint transitions, concomitant with a marked increase of the positive cell cycle regulators, including cyclin D1, cyclin A and cyclin B1. HPIP inhibits CRC cell apoptosis accompanied by the decreased levels of BAX and PIG3, the inducers of apoptosis and the increased level of the apoptosis inhibitor BCL2. HPIP blocks caspase-3-mediated cleavage of PARP, an important apoptosis marker. HPIP promotes CRC cell migration and invasion and regulates epithelial-mesenchymal transition (EMT), which plays a critical role in cancer cell migration and invasion. Activation of MAPK/ERK1/2 and PI3k/AKT pathways is required for HPIP modulation of CRC cell proliferation, migration and EMT. Moreover, HPIP knockdown suppresses colorectal tumor growth in nude mice. These data highlight the important role of HPIP in CRC cell proliferation and progression and suggest that HPIP may be a useful target for CRC therapy.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>25800793</pmid><doi>10.1038/srep09429</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2045-2322 |
ispartof | Scientific reports, 2015-03, Vol.5 (1), p.9429-9429, Article 9429 |
issn | 2045-2322 2045-2322 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4371107 |
source | Publicly Available Content Database; Full-Text Journals in Chemistry (Open access); PubMed; Springer Nature - nature.com Journals - Fully Open Access |
subjects | 1-Phosphatidylinositol 3-kinase 13/109 13/2 13/31 13/51 13/89 38/88 45/44 631/67/1504 631/67/395 64/60 82/1 82/80 96/106 AKT protein Animals Apoptosis Apoptosis - genetics BAX protein Caspase Caspase-3 Cell activation Cell adhesion & migration Cell cycle Cell Cycle - genetics Cell Cycle Proteins - genetics Cell Cycle Proteins - metabolism Cell growth Cell Line, Tumor Cell migration Cell Movement - genetics Cell Proliferation Colorectal cancer Colorectal carcinoma Colorectal Neoplasms - genetics Colorectal Neoplasms - metabolism Colorectal Neoplasms - pathology Cyclin A Cyclin B1 Cyclin D1 Disease Models, Animal Epithelial-Mesenchymal Transition Gene Expression Gene Knockdown Techniques Heterografts Humanities and Social Sciences Humans Intracellular Signaling Peptides and Proteins - genetics Intracellular Signaling Peptides and Proteins - metabolism Leukemia Lymphocytes B MAP kinase Mesenchyme Mice Mitogen-Activated Protein Kinases - metabolism multidisciplinary Poly(ADP-ribose) polymerase Proto-Oncogene Proteins c-akt - metabolism Science Up-Regulation |
title | HPIP is upregulated in colorectal cancer and regulates colorectal cancer cell proliferation, apoptosis and invasion |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T17%3A42%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=HPIP%20is%20upregulated%20in%20colorectal%20cancer%20and%20regulates%20colorectal%20cancer%20cell%20proliferation,%20apoptosis%20and%20invasion&rft.jtitle=Scientific%20reports&rft.au=Feng,%20Yingying&rft.date=2015-03-24&rft.volume=5&rft.issue=1&rft.spage=9429&rft.epage=9429&rft.pages=9429-9429&rft.artnum=9429&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/srep09429&rft_dat=%3Cproquest_pubme%3E1666723515%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c504t-e75021071f2ab3b71ff64e2412bc88e83ed4e29f25077c97b5ee261b95246e3c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1898634577&rft_id=info:pmid/25800793&rfr_iscdi=true |