Infiltration of thymidine phosphorylase-positive macrophages is closely associated with tumor angiogenesis and survival in intestinal type gastric cancer

Akihiko Kawahara, Satoshi Hattori, Jun Akiba, Kazutaka Nakashima, Tomoki Taira, Kosuke Watari, Fumihito Hosoi, Manami Uba, Yuji Basaki, Kikuo Koufuji, Kazuo Shirouzu, Shin Ichi Akiyama, Michihiko Kuwano, Masayoshi Kage, Mayumi Ono

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38 Citations (Scopus)

Abstract

Thymidine phosphorylase (TP), an enzyme catalyzing the reversible phospholysis of thymidine, deoxyuridine and their analogs at their respective bases and 2-deoxyribose-1-phosphate, thus promoting angiogenesis, is often expressed in macrophages present in tumor stroma. In this study, we investigated whether infiltration of TP-positive macrophages as well as tumor-associated macrophages affected tumor angiogenesis. TP was expressed in human macrophage-like cells, but not in gastric cancer cells in culture. The expression level of TP, the number of infiltrating CD68+ and CD163+ macrophages, and microvessel density (MVD) in the tumor were further analyzed by immunohistochemistry in 111 patients with gastric cancer. Biostatistical analysis of digitized data obtained by image analysis showed that TP expression was significantly correlated with the number of infiltrating macrophages and MVD in intestinal type gastric cancer (p<0.05). The number of infiltrating macrophages was also correlated with MVD in both the intestinal and diffuse types (p<0.05). An increased number of CD68+ macrophages was significantly associated with poor outcome in patients with intestinal type (p<0.001), but not diffuse type cancer. TP could be a specific marker enzyme that is expressed in tumor-infiltrating macrophages, being associated with tumor angiogenesis and poor prognosis in patients with intestinal-type gastric cancer.

Original languageEnglish
Pages (from-to)405-415
Number of pages11
JournalOncology reports
Volume24
Issue number2
DOIs
Publication statusPublished - Aug 2010

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All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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