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Sökning: WFRF:(Huhta H) > (2015-2019) > Intratumoral lactat...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003524naa a2200445 4500
001oai:openarchive.ki.se:10616/45901
003SwePub
008240410s2017 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:135591907
022 a 1949-2553
024a 10616/459012 hdl
024a http://hdl.handle.net/10616/459012 URI
024a https://doi.org/10.18632/oncotarget.152842 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1355919072 URI
040 a (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Kauppila, Joonas Hu Karolinska Institutet4 aut
2451 0a Intratumoral lactate metabolism in Barrett’s esophagus and adenocarcinoma
264 c 2017-02-11
264 1a Stockholm :b Karolinska Institutet, Dept of Molecular Medicine and Surgery,c 2017
338 a electronic2 rdacarrier
520 a Background: Monocarboxylate transporters (MCTs) are cell membrane proteins which transport pyruvate, lactate and ketone bodies across the plasma membrane. MCTs are activated in various cancers, but their expression in esophageal adenocarcinoma is not known. The present study was conducted to elucidate the expression of MCTs in esophageal adenocarcinoma and its precursor lesions. Results: Cytoplasmic MCT1, MCT4 and MTCO1 expression linearly increased from normal epithelium to Barrett's mucosa to dysplasia and cancer. Low cytoplasmic MCT1 expression associated with high T-class (P < 0.01), positive lymph node metastases (P < 0.05), positive distant metastases (P < 0.01) and high tumor stage (P < 0.01). High cytoplasmic MCT4 expression correlated significantly with positive distant metastases (P < 0.05). Both low MCT1 and high MCT4 histoscore predicted survival in univariate analysis (P < 0.01). MCT4 histoscore predicted survival in multivariate analysis (P = 0.043; HR 1.8 95%CI 1.0–3.1). MTCO1 expression was not correlated to clinicopathological variables or survival. Materials and Methods: MCT1, MCT4 and mitochondrial cytochrome c oxidase (MTCO1) expression were determined with immunohistochemistry in esophageal specimens from 129 patients with columnar dysplasia or adenocarcinoma. Specimens including normal esophagus (n = 88), gastric (n = 67) or intestinal metaplasia (n = 51), low-grade (n = 42), high-grade dysplasia (n = 37) and esophageal adenocarcinoma (n = 99) were evaluated. Conclusions: Major increase in markers of tumor metabolism occurs during carcinogenesis and progression of esophageal adenocarcinoma. MCT1 and MCT4 are prognostic factors in esophageal adenocarcinoma.
700a Huhta, Heikki4 aut
700a Helminen, Olli4 aut
700a Palomäki, Sami4 aut
700a Lehenkari, Petri4 aut
700a Saarnio, Juha4 aut
700a Karttunen, Tuomo4 aut
710a Karolinska Institutet
710a Karolinska Institutet
710a Karolinska Institutet4 org
773t Oncotargetd Stockholm : Karolinska Institutet, Dept of Molecular Medicine and Surgeryx 1949-2553
856u http://hdl.handle.net/10616/45901x primaryx Object in contextx freey FULLTEXT
856u http://www.oncotarget.com/index.php?journal=oncotarget&page=article&op=download&path%5B%5D=15284&path%5B%5D=48856
8564 8u http://hdl.handle.net/10616/45901
8564 8u https://doi.org/10.18632/oncotarget.15284
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:135591907

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