Urokinase plasminogen activator receptor is expressed in invasive cells in gastric carcinomas from high- and low-risk countries

被引:27
作者
Alpizar-Alpizar, Warner [1 ,2 ,3 ,4 ]
Nielsen, Boye Schnack [4 ]
Sierra, Rafaela [3 ]
Illemann, Martin [4 ]
Ramirez, Jose A. [5 ]
Arias, Adriana [5 ]
Duran, Sundry [6 ]
Skarstein, Arne [7 ,8 ]
Ovrebo, Kjell [7 ,8 ]
Lund, Leif R. [9 ]
Laerum, Ole D. [2 ]
机构
[1] Haukeland Hosp, Gade Inst, Dept Pathol, N-5021 Bergen, Norway
[2] Univ Bergen, Gade Inst, Bergen, Norway
[3] Univ Costa Rica, Canc Res Program, Hlth Res Inst INISA, San Jose, Costa Rica
[4] Rigshosp, Finsen Lab, DK-2100 Copenhagen, Denmark
[5] Dr Rafael A Calderon Guardia Hosp, Dept Pathol, San Jose, Costa Rica
[6] Dr Max Peralta Hosp, Dept Pathol, Cartago, Costa Rica
[7] Haukeland Hosp, Dept Surg, N-5021 Bergen, Norway
[8] Univ Bergen, Dept Surg Sci, Bergen, Norway
[9] Univ Copenhagen, Sect Cell & Dev Biol, Dept Biol, Copenhagen, Denmark
关键词
uPAR; gastric cancer; Helicobacter pylori; gastritis; immunohistochemistry; TUMOR-ASSOCIATED PROTEASES; MINIMAL RESIDUAL DISEASE; HELICOBACTER-PYLORI; STROMAL CELLS; PROGNOSTIC IMPACT; GROWTH-FACTOR; CANCER-CELLS; BONE-MARROW; INHIBITOR-1; DORMANCY;
D O I
10.1002/ijc.24755
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gastric cancer is the second cancer causing death worldwide. Both incidence and mortality rates vary according to geographical regions. The receptor for urokinase plasminogen activator (uPAR) is involved in extracellular matrix degradation by mediating cell surface associated plasminogen activation, and its presence on gastric cancer cells is linked to micro-metastasis and poor prognosis. Immunohistochemical analyses of a set of 44 gastric cancer lesions from Costa Rica showed expression of uPAR in cancer cells in both intestinal subtype (14 of 27) and diffuse subtype (10 of 17). We compared the expression pattern of uPAR in gastric cancers from a high-risk country (Costa Rica) with a low-risk country (Norway). We found uPAR on gastric cancer cells in 24 of 44 cases (54%) from Costa Rica and in 13 of 23 cases (56%) from Norway. uPAR was seen in macrophages and neutrophils in all cases. We also examined the nonneoplastic mucosa and found that uPAR was more frequently seen in epithelial cells located at the luminal edge of the crypts in cases with Helicobacter pylori infection than in similar epithelial cells in noninfected mucosa (p = 0.033; chi(2) = 4.54). In conclusion, the expression of uPAR in cancer cells in more than half of the gastric cancer cases suggests that their uPAR-positivity do not contribute to explain the different mortality rates between the 2 countries, however, the actual prevalence of uPAR-positive cancer cells in the gastric cancers may still provide prognostic information.
引用
收藏
页码:405 / 415
页数:11
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