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Overexpression of SIP1 and Downregulation of E-cadherin Predict Delayed Neck Metastasis in Stage I/II Oral Tongue Squamous Cell Carcinoma After Partial Glossectomy
Background Patients with clinical stage I/II (T1–2N0M0) oral tongue squamous cell carcinoma (TSCC) usually undergo partial glossectomy alone. However, 14–48% of them develop delayed neck metastasis (DNM), which may lead to an unfavorable course. Recently epithelial-to-mesenchymal transition (EMT) ha...
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Published in: | Annals of surgical oncology 2012-02, Vol.19 (2), p.612-619 |
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creator | Sakamoto, Koji Imanishi, Yorihisa Tomita, Toshiki Shimoda, Masayuki Kameyama, Kaori Shibata, Katsushi Sakai, Nobuya Ozawa, Hiroyuki Shigetomi, Seiji Fujii, Ryoichi Fujii, Masato Ogawa, Kaoru |
description | Background
Patients with clinical stage I/II (T1–2N0M0) oral tongue squamous cell carcinoma (TSCC) usually undergo partial glossectomy alone. However, 14–48% of them develop delayed neck metastasis (DNM), which may lead to an unfavorable course. Recently epithelial-to-mesenchymal transition (EMT) has been thought to play a crucial role in cancer metastasis. The present study aimed to examine the associations of EMT-involved molecular factors and clinicopathological factors with DNM in stage I/II TSCC.
Methods
mRNA expression levels of E-cadherin and its transcriptional repressors (snail, SIP1, and twist) in 7 head and neck squamous cell carcinoma (HNSCC) cell lines were evaluated by quantitative real-time PCR. Clinicopathological parameters and immunohistochemical expressions of E-cadherin and its repressors were examined in surgical specimens of 37 stage I/II TSCC patients who underwent partial glossectomy alone.
Results
In HNSCC cells, E-cadherin expression was inversely correlated with SIP1 expression (
P
= 0.023). Univariate analysis of immunohistochemistry showed that overexpression of SIP1 and loss of E-cadherin were significantly correlated with DNM, although no inverse correlation was found between E-cadherin and its repressors. Multiple logistic regression analysis including clinicopathological and molecular factors revealed that overexpression of SIP1 (
P
= 0.005), loss of E-cadherin (
P
= 0.046), and vascular invasion (
P
= 0.024) were independently correlated with DNM.
Conclusions
These results suggest that development of DNM in stage I/II TSCC is closely related to induction of EMT in primary tumor cells. Especially, SIP1 and E-cadherin are considered to be the possible markers for selecting patients at high risk of DNM. |
doi_str_mv | 10.1245/s10434-011-2052-1 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_917858403</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2568194151</sourcerecordid><originalsourceid>FETCH-LOGICAL-c436t-3b6c132757c6236793dff42407e281467818eed73e2504fcf0ddd3a6153baf273</originalsourceid><addsrcrecordid>eNp1kd1uEzEQhS0EoqXlAbhBFje92tZje_8uq7S0KxUSKeXacuzZsGXXTu1dIM_Di9ZRUpCQKlmy5fnmzLEPIR-AnQOX-UUEJoXMGEDGWc4zeEWOIU83sqjgdTqzospqXuRH5F2MD4xBKVj-lhxxqEEwEMfkz_wnBvy9CRhj5x31LV02C6DaWXrlf7mA66nX46F0nRltv2PoHF0EtJ0Z6RX2eouWfkXzg37BUce0ukgTshz1Gmlz0TR0HnRP771bT0iXj5Me_BTpDPueznQwnfODppftiIEudBi7BN_0PkY0ox-2p-RNq_uI7w_7Cfn2-fp-dpvdzW-a2eVdZqQoxkysCgOCl3lpCi6Ksha2bSWXrERegSzKCipEWwrkOZOtaZm1Vugi_dhKt7wUJ-Rsr7sJ_nHCOKqhiyaZ1A6TX1VDWeWVZCKRn_4jH_wUXDK3gwRUIOoEwR4yIT0lYKs2oRt02Cpgapef2uenUn5ql5-C1PPxIDytBrR_O54DSwDfAzGV3BrDv8kvqz4B_BOlew</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>917318139</pqid></control><display><type>article</type><title>Overexpression of SIP1 and Downregulation of E-cadherin Predict Delayed Neck Metastasis in Stage I/II Oral Tongue Squamous Cell Carcinoma After Partial Glossectomy</title><source>Springer Link</source><creator>Sakamoto, Koji ; Imanishi, Yorihisa ; Tomita, Toshiki ; Shimoda, Masayuki ; Kameyama, Kaori ; Shibata, Katsushi ; Sakai, Nobuya ; Ozawa, Hiroyuki ; Shigetomi, Seiji ; Fujii, Ryoichi ; Fujii, Masato ; Ogawa, Kaoru</creator><creatorcontrib>Sakamoto, Koji ; Imanishi, Yorihisa ; Tomita, Toshiki ; Shimoda, Masayuki ; Kameyama, Kaori ; Shibata, Katsushi ; Sakai, Nobuya ; Ozawa, Hiroyuki ; Shigetomi, Seiji ; Fujii, Ryoichi ; Fujii, Masato ; Ogawa, Kaoru</creatorcontrib><description>Background
Patients with clinical stage I/II (T1–2N0M0) oral tongue squamous cell carcinoma (TSCC) usually undergo partial glossectomy alone. However, 14–48% of them develop delayed neck metastasis (DNM), which may lead to an unfavorable course. Recently epithelial-to-mesenchymal transition (EMT) has been thought to play a crucial role in cancer metastasis. The present study aimed to examine the associations of EMT-involved molecular factors and clinicopathological factors with DNM in stage I/II TSCC.
Methods
mRNA expression levels of E-cadherin and its transcriptional repressors (snail, SIP1, and twist) in 7 head and neck squamous cell carcinoma (HNSCC) cell lines were evaluated by quantitative real-time PCR. Clinicopathological parameters and immunohistochemical expressions of E-cadherin and its repressors were examined in surgical specimens of 37 stage I/II TSCC patients who underwent partial glossectomy alone.
Results
In HNSCC cells, E-cadherin expression was inversely correlated with SIP1 expression (
P
= 0.023). Univariate analysis of immunohistochemistry showed that overexpression of SIP1 and loss of E-cadherin were significantly correlated with DNM, although no inverse correlation was found between E-cadherin and its repressors. Multiple logistic regression analysis including clinicopathological and molecular factors revealed that overexpression of SIP1 (
P
= 0.005), loss of E-cadherin (
P
= 0.046), and vascular invasion (
P
= 0.024) were independently correlated with DNM.
Conclusions
These results suggest that development of DNM in stage I/II TSCC is closely related to induction of EMT in primary tumor cells. Especially, SIP1 and E-cadherin are considered to be the possible markers for selecting patients at high risk of DNM.</description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1245/s10434-011-2052-1</identifier><identifier>PMID: 21913013</identifier><language>eng</language><publisher>New York: Springer-Verlag</publisher><subject>Biomarkers, Tumor - genetics ; Biomarkers, Tumor - metabolism ; Blotting, Western ; Cadherins - genetics ; Cadherins - metabolism ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - metabolism ; Carcinoma, Squamous Cell - surgery ; Down-Regulation ; Epithelial-Mesenchymal Transition ; Female ; Gene Expression Regulation, Neoplastic ; Glossectomy ; Head and Neck Oncology ; Humans ; Immunoenzyme Techniques ; Lymph Node Excision ; Lymphatic Metastasis ; Male ; Medical Records ; Medicine ; Medicine & Public Health ; Middle Aged ; Neoplasm Invasiveness ; Neoplasm Staging ; Nerve Tissue Proteins - genetics ; Nerve Tissue Proteins - metabolism ; Oncology ; Prognosis ; Real-Time Polymerase Chain Reaction ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - genetics ; RNA-Binding Proteins - genetics ; RNA-Binding Proteins - metabolism ; Surgery ; Surgical Oncology ; Tongue Neoplasms - genetics ; Tongue Neoplasms - metabolism ; Tongue Neoplasms - surgery ; Tumor Cells, Cultured</subject><ispartof>Annals of surgical oncology, 2012-02, Vol.19 (2), p.612-619</ispartof><rights>Society of Surgical Oncology 2011</rights><rights>Society of Surgical Oncology 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-3b6c132757c6236793dff42407e281467818eed73e2504fcf0ddd3a6153baf273</citedby><cites>FETCH-LOGICAL-c436t-3b6c132757c6236793dff42407e281467818eed73e2504fcf0ddd3a6153baf273</cites></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/21913013$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sakamoto, Koji</creatorcontrib><creatorcontrib>Imanishi, Yorihisa</creatorcontrib><creatorcontrib>Tomita, Toshiki</creatorcontrib><creatorcontrib>Shimoda, Masayuki</creatorcontrib><creatorcontrib>Kameyama, Kaori</creatorcontrib><creatorcontrib>Shibata, Katsushi</creatorcontrib><creatorcontrib>Sakai, Nobuya</creatorcontrib><creatorcontrib>Ozawa, Hiroyuki</creatorcontrib><creatorcontrib>Shigetomi, Seiji</creatorcontrib><creatorcontrib>Fujii, Ryoichi</creatorcontrib><creatorcontrib>Fujii, Masato</creatorcontrib><creatorcontrib>Ogawa, Kaoru</creatorcontrib><title>Overexpression of SIP1 and Downregulation of E-cadherin Predict Delayed Neck Metastasis in Stage I/II Oral Tongue Squamous Cell Carcinoma After Partial Glossectomy</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><addtitle>Ann Surg Oncol</addtitle><description>Background
Patients with clinical stage I/II (T1–2N0M0) oral tongue squamous cell carcinoma (TSCC) usually undergo partial glossectomy alone. However, 14–48% of them develop delayed neck metastasis (DNM), which may lead to an unfavorable course. Recently epithelial-to-mesenchymal transition (EMT) has been thought to play a crucial role in cancer metastasis. The present study aimed to examine the associations of EMT-involved molecular factors and clinicopathological factors with DNM in stage I/II TSCC.
Methods
mRNA expression levels of E-cadherin and its transcriptional repressors (snail, SIP1, and twist) in 7 head and neck squamous cell carcinoma (HNSCC) cell lines were evaluated by quantitative real-time PCR. Clinicopathological parameters and immunohistochemical expressions of E-cadherin and its repressors were examined in surgical specimens of 37 stage I/II TSCC patients who underwent partial glossectomy alone.
Results
In HNSCC cells, E-cadherin expression was inversely correlated with SIP1 expression (
P
= 0.023). Univariate analysis of immunohistochemistry showed that overexpression of SIP1 and loss of E-cadherin were significantly correlated with DNM, although no inverse correlation was found between E-cadherin and its repressors. Multiple logistic regression analysis including clinicopathological and molecular factors revealed that overexpression of SIP1 (
P
= 0.005), loss of E-cadherin (
P
= 0.046), and vascular invasion (
P
= 0.024) were independently correlated with DNM.
Conclusions
These results suggest that development of DNM in stage I/II TSCC is closely related to induction of EMT in primary tumor cells. Especially, SIP1 and E-cadherin are considered to be the possible markers for selecting patients at high risk of DNM.</description><subject>Biomarkers, Tumor - genetics</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Blotting, Western</subject><subject>Cadherins - genetics</subject><subject>Cadherins - metabolism</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Carcinoma, Squamous Cell - surgery</subject><subject>Down-Regulation</subject><subject>Epithelial-Mesenchymal Transition</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Glossectomy</subject><subject>Head and Neck Oncology</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Lymph Node Excision</subject><subject>Lymphatic Metastasis</subject><subject>Male</subject><subject>Medical Records</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Staging</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Oncology</subject><subject>Prognosis</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - genetics</subject><subject>RNA-Binding Proteins - genetics</subject><subject>RNA-Binding Proteins - metabolism</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Tongue Neoplasms - genetics</subject><subject>Tongue Neoplasms - metabolism</subject><subject>Tongue Neoplasms - surgery</subject><subject>Tumor Cells, Cultured</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp1kd1uEzEQhS0EoqXlAbhBFje92tZje_8uq7S0KxUSKeXacuzZsGXXTu1dIM_Di9ZRUpCQKlmy5fnmzLEPIR-AnQOX-UUEJoXMGEDGWc4zeEWOIU83sqjgdTqzospqXuRH5F2MD4xBKVj-lhxxqEEwEMfkz_wnBvy9CRhj5x31LV02C6DaWXrlf7mA66nX46F0nRltv2PoHF0EtJ0Z6RX2eouWfkXzg37BUce0ukgTshz1Gmlz0TR0HnRP771bT0iXj5Me_BTpDPueznQwnfODppftiIEudBi7BN_0PkY0ox-2p-RNq_uI7w_7Cfn2-fp-dpvdzW-a2eVdZqQoxkysCgOCl3lpCi6Ksha2bSWXrERegSzKCipEWwrkOZOtaZm1Vugi_dhKt7wUJ-Rsr7sJ_nHCOKqhiyaZ1A6TX1VDWeWVZCKRn_4jH_wUXDK3gwRUIOoEwR4yIT0lYKs2oRt02Cpgapef2uenUn5ql5-C1PPxIDytBrR_O54DSwDfAzGV3BrDv8kvqz4B_BOlew</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Sakamoto, Koji</creator><creator>Imanishi, Yorihisa</creator><creator>Tomita, Toshiki</creator><creator>Shimoda, Masayuki</creator><creator>Kameyama, Kaori</creator><creator>Shibata, Katsushi</creator><creator>Sakai, Nobuya</creator><creator>Ozawa, Hiroyuki</creator><creator>Shigetomi, Seiji</creator><creator>Fujii, Ryoichi</creator><creator>Fujii, Masato</creator><creator>Ogawa, Kaoru</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><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>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20120201</creationdate><title>Overexpression of SIP1 and Downregulation of E-cadherin Predict Delayed Neck Metastasis in Stage I/II Oral Tongue Squamous Cell Carcinoma After Partial Glossectomy</title><author>Sakamoto, Koji ; Imanishi, Yorihisa ; Tomita, Toshiki ; Shimoda, Masayuki ; Kameyama, Kaori ; Shibata, Katsushi ; Sakai, Nobuya ; Ozawa, Hiroyuki ; Shigetomi, Seiji ; Fujii, Ryoichi ; Fujii, Masato ; Ogawa, Kaoru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-3b6c132757c6236793dff42407e281467818eed73e2504fcf0ddd3a6153baf273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Biomarkers, Tumor - genetics</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Blotting, Western</topic><topic>Cadherins - genetics</topic><topic>Cadherins - metabolism</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Carcinoma, Squamous Cell - surgery</topic><topic>Down-Regulation</topic><topic>Epithelial-Mesenchymal Transition</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Glossectomy</topic><topic>Head and Neck Oncology</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Lymph Node Excision</topic><topic>Lymphatic Metastasis</topic><topic>Male</topic><topic>Medical Records</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Staging</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Oncology</topic><topic>Prognosis</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - genetics</topic><topic>RNA-Binding Proteins - genetics</topic><topic>RNA-Binding Proteins - metabolism</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><topic>Tongue Neoplasms - genetics</topic><topic>Tongue Neoplasms - metabolism</topic><topic>Tongue Neoplasms - surgery</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sakamoto, Koji</creatorcontrib><creatorcontrib>Imanishi, Yorihisa</creatorcontrib><creatorcontrib>Tomita, Toshiki</creatorcontrib><creatorcontrib>Shimoda, Masayuki</creatorcontrib><creatorcontrib>Kameyama, Kaori</creatorcontrib><creatorcontrib>Shibata, Katsushi</creatorcontrib><creatorcontrib>Sakai, Nobuya</creatorcontrib><creatorcontrib>Ozawa, Hiroyuki</creatorcontrib><creatorcontrib>Shigetomi, Seiji</creatorcontrib><creatorcontrib>Fujii, Ryoichi</creatorcontrib><creatorcontrib>Fujii, Masato</creatorcontrib><creatorcontrib>Ogawa, Kaoru</creatorcontrib><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>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma 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 Central UK/Ireland</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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 China</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sakamoto, Koji</au><au>Imanishi, Yorihisa</au><au>Tomita, Toshiki</au><au>Shimoda, Masayuki</au><au>Kameyama, Kaori</au><au>Shibata, Katsushi</au><au>Sakai, Nobuya</au><au>Ozawa, Hiroyuki</au><au>Shigetomi, Seiji</au><au>Fujii, Ryoichi</au><au>Fujii, Masato</au><au>Ogawa, Kaoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overexpression of SIP1 and Downregulation of E-cadherin Predict Delayed Neck Metastasis in Stage I/II Oral Tongue Squamous Cell Carcinoma After Partial Glossectomy</atitle><jtitle>Annals of surgical oncology</jtitle><stitle>Ann Surg Oncol</stitle><addtitle>Ann Surg Oncol</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>19</volume><issue>2</issue><spage>612</spage><epage>619</epage><pages>612-619</pages><issn>1068-9265</issn><eissn>1534-4681</eissn><abstract>Background
Patients with clinical stage I/II (T1–2N0M0) oral tongue squamous cell carcinoma (TSCC) usually undergo partial glossectomy alone. However, 14–48% of them develop delayed neck metastasis (DNM), which may lead to an unfavorable course. Recently epithelial-to-mesenchymal transition (EMT) has been thought to play a crucial role in cancer metastasis. The present study aimed to examine the associations of EMT-involved molecular factors and clinicopathological factors with DNM in stage I/II TSCC.
Methods
mRNA expression levels of E-cadherin and its transcriptional repressors (snail, SIP1, and twist) in 7 head and neck squamous cell carcinoma (HNSCC) cell lines were evaluated by quantitative real-time PCR. Clinicopathological parameters and immunohistochemical expressions of E-cadherin and its repressors were examined in surgical specimens of 37 stage I/II TSCC patients who underwent partial glossectomy alone.
Results
In HNSCC cells, E-cadherin expression was inversely correlated with SIP1 expression (
P
= 0.023). Univariate analysis of immunohistochemistry showed that overexpression of SIP1 and loss of E-cadherin were significantly correlated with DNM, although no inverse correlation was found between E-cadherin and its repressors. Multiple logistic regression analysis including clinicopathological and molecular factors revealed that overexpression of SIP1 (
P
= 0.005), loss of E-cadherin (
P
= 0.046), and vascular invasion (
P
= 0.024) were independently correlated with DNM.
Conclusions
These results suggest that development of DNM in stage I/II TSCC is closely related to induction of EMT in primary tumor cells. Especially, SIP1 and E-cadherin are considered to be the possible markers for selecting patients at high risk of DNM.</abstract><cop>New York</cop><pub>Springer-Verlag</pub><pmid>21913013</pmid><doi>10.1245/s10434-011-2052-1</doi><tpages>8</tpages></addata></record> |
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source | Springer Link |
subjects | Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism Blotting, Western Cadherins - genetics Cadherins - metabolism Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - metabolism Carcinoma, Squamous Cell - surgery Down-Regulation Epithelial-Mesenchymal Transition Female Gene Expression Regulation, Neoplastic Glossectomy Head and Neck Oncology Humans Immunoenzyme Techniques Lymph Node Excision Lymphatic Metastasis Male Medical Records Medicine Medicine & Public Health Middle Aged Neoplasm Invasiveness Neoplasm Staging Nerve Tissue Proteins - genetics Nerve Tissue Proteins - metabolism Oncology Prognosis Real-Time Polymerase Chain Reaction Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - genetics RNA-Binding Proteins - genetics RNA-Binding Proteins - metabolism Surgery Surgical Oncology Tongue Neoplasms - genetics Tongue Neoplasms - metabolism Tongue Neoplasms - surgery Tumor Cells, Cultured |
title | Overexpression of SIP1 and Downregulation of E-cadherin Predict Delayed Neck Metastasis in Stage I/II Oral Tongue Squamous Cell Carcinoma After Partial Glossectomy |
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