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Increased expression of system large amino acid transporter (LAT)-1 mRNA is associated with invasive potential and unfavorable prognosis of human clear cell renal cell carcinoma

The system L amino acid transporter (LAT) has an important role in the transport of various amino acids, and there have been reports about the relation of this system to cancer. Although LATs are highly expressed in the kidneys, little is known about their influence on human renal cancer. To clarify...

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Published in:BMC cancer 2013-10, Vol.13 (1), p.509-509, Article 509
Main Authors: Betsunoh, Hironori, Fukuda, Takehiko, Anzai, Naohiko, Nishihara, Daisaku, Mizuno, Tomoya, Yuki, Hideo, Masuda, Akinori, Yamaguchi, Yoshiyuki, Abe, Hideyuki, Yashi, Masahiro, Fukabori, Yoshitatsu, Yoshida, Ken-Ichiro, Kamai, Takao
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container_title BMC cancer
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creator Betsunoh, Hironori
Fukuda, Takehiko
Anzai, Naohiko
Nishihara, Daisaku
Mizuno, Tomoya
Yuki, Hideo
Masuda, Akinori
Yamaguchi, Yoshiyuki
Abe, Hideyuki
Yashi, Masahiro
Fukabori, Yoshitatsu
Yoshida, Ken-Ichiro
Kamai, Takao
description The system L amino acid transporter (LAT) has an important role in the transport of various amino acids, and there have been reports about the relation of this system to cancer. Although LATs are highly expressed in the kidneys, little is known about their influence on human renal cancer. To clarify the role of LATs in human clear cell renal cell carcinoma (RCC), we investigated the expression of mRNAs for LAT1, LAT2, LAT3, LAT4, and 4F2hc in clear cell RCC tissues. The mRNAs of these five genes were analyzed by the real-time reverse transcription polymerase chain reaction in matched sets of tumor and non-tumor tissues obtained at operation from 82 Japanese patients with clear cell RCC. We also measured phosphorylated S6 ribosomal protein (Ser-235/236) proteins levels in 18 paired tumor and non-tumor tissues of the patients by Western blotting. Expression of LAT1 mRNA was significantly increased in tumor tissue compared with non-tumor tissue, while expression of LAT2 and LAT3 mRNAs was reduced. There was no difference in the expression of LAT4 and 4F2hc mRNAs between tumor and non-tumor tissues. Increased expression of LAT1 mRNA was associated with less differentiated tumors, local invasion, microscopic vascular invasion, and metastasis. Kaplan-Meier survival analysis showed that a higher serum LAT1 mRNA level was associated with a shorter overall survival time. Phosphorylated S6 ribosomal protein levels were associated with metastatic potential. LAT1 mRNA levels positively correlated with phosphorylated S6 ribosomal protein proteins levels in primary tumors. These findings suggest that LAT1 mRNA is related to the invasive and progressive potential of clear cell RCC.
doi_str_mv 10.1186/1471-2407-13-509
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Although LATs are highly expressed in the kidneys, little is known about their influence on human renal cancer. To clarify the role of LATs in human clear cell renal cell carcinoma (RCC), we investigated the expression of mRNAs for LAT1, LAT2, LAT3, LAT4, and 4F2hc in clear cell RCC tissues. The mRNAs of these five genes were analyzed by the real-time reverse transcription polymerase chain reaction in matched sets of tumor and non-tumor tissues obtained at operation from 82 Japanese patients with clear cell RCC. We also measured phosphorylated S6 ribosomal protein (Ser-235/236) proteins levels in 18 paired tumor and non-tumor tissues of the patients by Western blotting. Expression of LAT1 mRNA was significantly increased in tumor tissue compared with non-tumor tissue, while expression of LAT2 and LAT3 mRNAs was reduced. There was no difference in the expression of LAT4 and 4F2hc mRNAs between tumor and non-tumor tissues. Increased expression of LAT1 mRNA was associated with less differentiated tumors, local invasion, microscopic vascular invasion, and metastasis. Kaplan-Meier survival analysis showed that a higher serum LAT1 mRNA level was associated with a shorter overall survival time. Phosphorylated S6 ribosomal protein levels were associated with metastatic potential. LAT1 mRNA levels positively correlated with phosphorylated S6 ribosomal protein proteins levels in primary tumors. 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This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2013 Betsunoh et al.; licensee BioMed Central Ltd. 2013 Betsunoh et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b616t-e8a9c95cae6a110788c8ae0cc3858009c5bce0e37e2a3d9b01f39394619d742c3</citedby><cites>FETCH-LOGICAL-b616t-e8a9c95cae6a110788c8ae0cc3858009c5bce0e37e2a3d9b01f39394619d742c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3832879/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1459790692?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24168110$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Betsunoh, Hironori</creatorcontrib><creatorcontrib>Fukuda, Takehiko</creatorcontrib><creatorcontrib>Anzai, Naohiko</creatorcontrib><creatorcontrib>Nishihara, Daisaku</creatorcontrib><creatorcontrib>Mizuno, Tomoya</creatorcontrib><creatorcontrib>Yuki, Hideo</creatorcontrib><creatorcontrib>Masuda, Akinori</creatorcontrib><creatorcontrib>Yamaguchi, Yoshiyuki</creatorcontrib><creatorcontrib>Abe, Hideyuki</creatorcontrib><creatorcontrib>Yashi, Masahiro</creatorcontrib><creatorcontrib>Fukabori, Yoshitatsu</creatorcontrib><creatorcontrib>Yoshida, Ken-Ichiro</creatorcontrib><creatorcontrib>Kamai, Takao</creatorcontrib><title>Increased expression of system large amino acid transporter (LAT)-1 mRNA is associated with invasive potential and unfavorable prognosis of human clear cell renal cell carcinoma</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>The system L amino acid transporter (LAT) has an important role in the transport of various amino acids, and there have been reports about the relation of this system to cancer. 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Fukuda, Takehiko ; Anzai, Naohiko ; Nishihara, Daisaku ; Mizuno, Tomoya ; Yuki, Hideo ; Masuda, Akinori ; Yamaguchi, Yoshiyuki ; Abe, Hideyuki ; Yashi, Masahiro ; Fukabori, Yoshitatsu ; Yoshida, Ken-Ichiro ; Kamai, Takao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b616t-e8a9c95cae6a110788c8ae0cc3858009c5bce0e37e2a3d9b01f39394619d742c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Amino acids</topic><topic>Analysis</topic><topic>Cancer</topic><topic>Carcinoma, Renal cell</topic><topic>Carcinoma, Renal Cell - genetics</topic><topic>Carcinoma, Renal Cell - mortality</topic><topic>Carcinoma, Renal Cell - pathology</topic><topic>Carrier proteins</topic><topic>Diagnosis</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gene Expression</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Kidney Neoplasms - genetics</topic><topic>Kidney Neoplasms - mortality</topic><topic>Kidney Neoplasms - pathology</topic><topic>Large Neutral Amino Acid-Transporter 1 - genetics</topic><topic>Male</topic><topic>Messenger RNA</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Neoplasm Grading</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Metastasis</topic><topic>Neoplasm Staging</topic><topic>Patients</topic><topic>Phosphorylation</topic><topic>Prognosis</topic><topic>Proteins</topic><topic>Ribosomal Protein S6 - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>Rodents</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Betsunoh, Hironori</creatorcontrib><creatorcontrib>Fukuda, Takehiko</creatorcontrib><creatorcontrib>Anzai, Naohiko</creatorcontrib><creatorcontrib>Nishihara, Daisaku</creatorcontrib><creatorcontrib>Mizuno, Tomoya</creatorcontrib><creatorcontrib>Yuki, Hideo</creatorcontrib><creatorcontrib>Masuda, Akinori</creatorcontrib><creatorcontrib>Yamaguchi, Yoshiyuki</creatorcontrib><creatorcontrib>Abe, Hideyuki</creatorcontrib><creatorcontrib>Yashi, Masahiro</creatorcontrib><creatorcontrib>Fukabori, Yoshitatsu</creatorcontrib><creatorcontrib>Yoshida, Ken-Ichiro</creatorcontrib><creatorcontrib>Kamai, Takao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; 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Although LATs are highly expressed in the kidneys, little is known about their influence on human renal cancer. To clarify the role of LATs in human clear cell renal cell carcinoma (RCC), we investigated the expression of mRNAs for LAT1, LAT2, LAT3, LAT4, and 4F2hc in clear cell RCC tissues. The mRNAs of these five genes were analyzed by the real-time reverse transcription polymerase chain reaction in matched sets of tumor and non-tumor tissues obtained at operation from 82 Japanese patients with clear cell RCC. We also measured phosphorylated S6 ribosomal protein (Ser-235/236) proteins levels in 18 paired tumor and non-tumor tissues of the patients by Western blotting. Expression of LAT1 mRNA was significantly increased in tumor tissue compared with non-tumor tissue, while expression of LAT2 and LAT3 mRNAs was reduced. There was no difference in the expression of LAT4 and 4F2hc mRNAs between tumor and non-tumor tissues. Increased expression of LAT1 mRNA was associated with less differentiated tumors, local invasion, microscopic vascular invasion, and metastasis. Kaplan-Meier survival analysis showed that a higher serum LAT1 mRNA level was associated with a shorter overall survival time. Phosphorylated S6 ribosomal protein levels were associated with metastatic potential. LAT1 mRNA levels positively correlated with phosphorylated S6 ribosomal protein proteins levels in primary tumors. These findings suggest that LAT1 mRNA is related to the invasive and progressive potential of clear cell RCC.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>24168110</pmid><doi>10.1186/1471-2407-13-509</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1471-2407
ispartof BMC cancer, 2013-10, Vol.13 (1), p.509-509, Article 509
issn 1471-2407
1471-2407
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3832879
source Publicly Available Content (ProQuest); PubMed Central (Training)
subjects Adult
Aged
Aged, 80 and over
Amino acids
Analysis
Cancer
Carcinoma, Renal cell
Carcinoma, Renal Cell - genetics
Carcinoma, Renal Cell - mortality
Carcinoma, Renal Cell - pathology
Carrier proteins
Diagnosis
Female
Follow-Up Studies
Gene Expression
Health aspects
Humans
Kidney Neoplasms - genetics
Kidney Neoplasms - mortality
Kidney Neoplasms - pathology
Large Neutral Amino Acid-Transporter 1 - genetics
Male
Messenger RNA
Metastasis
Middle Aged
Neoplasm Grading
Neoplasm Invasiveness
Neoplasm Metastasis
Neoplasm Staging
Patients
Phosphorylation
Prognosis
Proteins
Ribosomal Protein S6 - metabolism
RNA, Messenger - genetics
Rodents
Tumors
title Increased expression of system large amino acid transporter (LAT)-1 mRNA is associated with invasive potential and unfavorable prognosis of human clear cell renal cell carcinoma
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