CXCR4 Expression in Gastric Cancer and Bone Marrow: Association with Hypoxia-Regulated Indices, Disseminated Tumor Cells, and Patients Survival

Aim. The analysis of the association of CXCR4 expression in gastric cancer (GC) and bone marrow (BM) with clinical characteristics. Patients and Methods. 65 patients with GC were investigated. Immunohistochemistry, immunocytochemistry, NMR-spectroscopy, and zymography were used. Results. CXCR4 was e...

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Veröffentlicht in:Journal of Cancer Research 2015-02, Vol.2015, p.1-8
Hauptverfasser: Osinsky, Dmitry, Kovelskaya, Antonina, Bubnovskaya, Larissa, Ganusevich, Irina, Gumenyuk, Lilya, Merentsev, Sergej, Osinsky, Sergej, Mamontova, Lesya
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container_title Journal of Cancer Research
container_volume 2015
creator Osinsky, Dmitry
Kovelskaya, Antonina
Bubnovskaya, Larissa
Ganusevich, Irina
Gumenyuk, Lilya
Merentsev, Sergej
Osinsky, Sergej
Mamontova, Lesya
description Aim. The analysis of the association of CXCR4 expression in gastric cancer (GC) and bone marrow (BM) with clinical characteristics. Patients and Methods. 65 patients with GC were investigated. Immunohistochemistry, immunocytochemistry, NMR-spectroscopy, and zymography were used. Results. CXCR4 was expressed in 78.5% of GC specimens and correlated with tumor hypoxia ( P < 0.05 ), VEGF expression ( P < 0.01 ), and gelatinases activity ( P < 0.05 ). CXCR4-positive cells in GC were detected in 80% of patients with disseminated tumor cells (DTCs). Overall survival (OS) of patients with CXCR4-positive tumors was poorer than that of patients with CXCR4-negative tumors ( P = 0.037 ). The CXCR4-positive cells in BM were found in 46% of all patients and in 56% of patients with DTCs. CXCR4 expression in BM was not associated with OS. Risk of unfavourable outcome is increased in patients with CXCR4-positive tumors ( P < 0.05 ). CXCR4 expression in BM was positively associated with DTCs, especially in patients with M0 category. Risk of unfavourable outcome is increased in patients with M 0 category and with both CXCR4-positive BM and DTCs ( P = 0.03 ). Conclusions. CXCR4 expression in tumor was positively correlated with hypoxia level and VEGF expression in tumor as well as OS. CXCR4 expression in BM is associated with DTCs.
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The analysis of the association of CXCR4 expression in gastric cancer (GC) and bone marrow (BM) with clinical characteristics. Patients and Methods. 65 patients with GC were investigated. Immunohistochemistry, immunocytochemistry, NMR-spectroscopy, and zymography were used. Results. CXCR4 was expressed in 78.5% of GC specimens and correlated with tumor hypoxia ( P &lt; 0.05 ), VEGF expression ( P &lt; 0.01 ), and gelatinases activity ( P &lt; 0.05 ). CXCR4-positive cells in GC were detected in 80% of patients with disseminated tumor cells (DTCs). Overall survival (OS) of patients with CXCR4-positive tumors was poorer than that of patients with CXCR4-negative tumors ( P = 0.037 ). The CXCR4-positive cells in BM were found in 46% of all patients and in 56% of patients with DTCs. CXCR4 expression in BM was not associated with OS. Risk of unfavourable outcome is increased in patients with CXCR4-positive tumors ( P &lt; 0.05 ). CXCR4 expression in BM was positively associated with DTCs, especially in patients with M0 category. Risk of unfavourable outcome is increased in patients with M 0 category and with both CXCR4-positive BM and DTCs ( P = 0.03 ). Conclusions. CXCR4 expression in tumor was positively correlated with hypoxia level and VEGF expression in tumor as well as OS. CXCR4 expression in BM is associated with DTCs.</description><identifier>ISSN: 2356-7201</identifier><identifier>EISSN: 2314-6915</identifier><identifier>DOI: 10.1155/2015/980214</identifier><language>eng</language><publisher>Hindawi Publishing Corporation</publisher><ispartof>Journal of Cancer Research, 2015-02, Vol.2015, p.1-8</ispartof><rights>Copyright © 2015 Dmitry Osinsky et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1084-b95e707b5350d5c85ce221cbad9c3ed5126b1b30b158e9fe7c4f0fd3915f154d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><contributor>Yoshida, Daizo</contributor><creatorcontrib>Osinsky, Dmitry</creatorcontrib><creatorcontrib>Kovelskaya, Antonina</creatorcontrib><creatorcontrib>Bubnovskaya, Larissa</creatorcontrib><creatorcontrib>Ganusevich, Irina</creatorcontrib><creatorcontrib>Gumenyuk, Lilya</creatorcontrib><creatorcontrib>Merentsev, Sergej</creatorcontrib><creatorcontrib>Osinsky, Sergej</creatorcontrib><creatorcontrib>Mamontova, Lesya</creatorcontrib><title>CXCR4 Expression in Gastric Cancer and Bone Marrow: Association with Hypoxia-Regulated Indices, Disseminated Tumor Cells, and Patients Survival</title><title>Journal of Cancer Research</title><description>Aim. The analysis of the association of CXCR4 expression in gastric cancer (GC) and bone marrow (BM) with clinical characteristics. Patients and Methods. 65 patients with GC were investigated. Immunohistochemistry, immunocytochemistry, NMR-spectroscopy, and zymography were used. Results. CXCR4 was expressed in 78.5% of GC specimens and correlated with tumor hypoxia ( P &lt; 0.05 ), VEGF expression ( P &lt; 0.01 ), and gelatinases activity ( P &lt; 0.05 ). CXCR4-positive cells in GC were detected in 80% of patients with disseminated tumor cells (DTCs). Overall survival (OS) of patients with CXCR4-positive tumors was poorer than that of patients with CXCR4-negative tumors ( P = 0.037 ). The CXCR4-positive cells in BM were found in 46% of all patients and in 56% of patients with DTCs. CXCR4 expression in BM was not associated with OS. Risk of unfavourable outcome is increased in patients with CXCR4-positive tumors ( P &lt; 0.05 ). CXCR4 expression in BM was positively associated with DTCs, especially in patients with M0 category. Risk of unfavourable outcome is increased in patients with M 0 category and with both CXCR4-positive BM and DTCs ( P = 0.03 ). Conclusions. CXCR4 expression in tumor was positively correlated with hypoxia level and VEGF expression in tumor as well as OS. 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The analysis of the association of CXCR4 expression in gastric cancer (GC) and bone marrow (BM) with clinical characteristics. Patients and Methods. 65 patients with GC were investigated. Immunohistochemistry, immunocytochemistry, NMR-spectroscopy, and zymography were used. Results. CXCR4 was expressed in 78.5% of GC specimens and correlated with tumor hypoxia ( P &lt; 0.05 ), VEGF expression ( P &lt; 0.01 ), and gelatinases activity ( P &lt; 0.05 ). CXCR4-positive cells in GC were detected in 80% of patients with disseminated tumor cells (DTCs). Overall survival (OS) of patients with CXCR4-positive tumors was poorer than that of patients with CXCR4-negative tumors ( P = 0.037 ). The CXCR4-positive cells in BM were found in 46% of all patients and in 56% of patients with DTCs. CXCR4 expression in BM was not associated with OS. Risk of unfavourable outcome is increased in patients with CXCR4-positive tumors ( P &lt; 0.05 ). CXCR4 expression in BM was positively associated with DTCs, especially in patients with M0 category. Risk of unfavourable outcome is increased in patients with M 0 category and with both CXCR4-positive BM and DTCs ( P = 0.03 ). Conclusions. CXCR4 expression in tumor was positively correlated with hypoxia level and VEGF expression in tumor as well as OS. CXCR4 expression in BM is associated with DTCs.</abstract><pub>Hindawi Publishing Corporation</pub><doi>10.1155/2015/980214</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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title CXCR4 Expression in Gastric Cancer and Bone Marrow: Association with Hypoxia-Regulated Indices, Disseminated Tumor Cells, and Patients Survival
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