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Th17 cells promote tumor growth in an immunocompetent orthotopic mouse model of prostate cancer.
Duan, Zhenling; Miller, Haiyan D; Fu, Xiaowei; Ge, Dongxia; Jin, Ben; Moustafa, Ahmed A; Lan, Ruoxin; Zhang, Kun; Chen, Zhenbang; You, Zongbing.
Affiliation
  • Duan Z; Department of Structural & Cellular Biology, Tulane University New Orleans, LA, USA.
  • Miller HD; Department of Gynecology, The First Affiliated Hospital of Kunming Medical University Kunming, China.
  • Fu X; Department of Structural & Cellular Biology, Tulane University New Orleans, LA, USA.
  • Ge D; Department of Structural & Cellular Biology, Tulane University New Orleans, LA, USA.
  • Jin B; Department of Clinical Medicine, The Second Affiliated Hospital, Shaanxi University of Chinese Medicine Xi'an, China.
  • Moustafa AA; Department of Structural & Cellular Biology, Tulane University New Orleans, LA, USA.
  • Lan R; Department of Structural & Cellular Biology, Tulane University New Orleans, LA, USA.
  • Zhang K; Department of Structural & Cellular Biology, Tulane University New Orleans, LA, USA.
  • Chen Z; Department of Structural & Cellular Biology, Tulane University New Orleans, LA, USA.
  • You Z; Department of Computer Science and Biostatistics Facility of RCMI Cancer Research Center, Xavier University of Louisiana New Orleans, LA, USA.
Am J Clin Exp Urol ; 7(4): 249-261, 2019.
Article de En | MEDLINE | ID: mdl-31511831
ABSTRACT
Interleukin-17 (IL-17) has been demonstrated to promote development of a variety of cancers including prostate cancer in genetically modified mouse models. IL-17 is the main product secreted by T helper 17 (Th17) cells. A recent study has shown that Th17 cells and related genes are upregulated in human prostate cancers. However, there is no direct experimental evidence to demonstrate Th17's role in prostate cancer. In the present study, we co-implanted mouse prostate cancer MPC3-luc cells with Th17-polarized mouse splenocytes in the prostate of immunocompetent C57BL/6J male mice. We found that Th17-polarized splenocytes promoted orthotopic allograft prostate tumor growth compared to the control splenocytes. The numbers of IL-17-positive lymphocytes and macrophages were higher in the prostate tumors grown from co-implantation of MPC3-luc cells and Th17-polarized splenocytes, compared to the prostate tumors grown from co-implantation of MPC3-luc cells and control splenocytes. Our findings provide the first direct experimental evidence that Th17 cells may promote prostate cancer growth.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Prognostic_studies Langue: En Journal: Am J Clin Exp Urol Année: 2019 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Prognostic_studies Langue: En Journal: Am J Clin Exp Urol Année: 2019 Type de document: Article Pays d'affiliation: États-Unis d'Amérique