Literature DB >> 16818694

Clinical significance of aminopeptidase N in non-small cell lung cancer.

Takahiro Tokuhara1, Noboru Hattori, Hisao Ishida, Tatsuya Hirai, Masahiko Higashiyama, Ken Kodama, Masayuki Miyake.   

Abstract

PURPOSE: The aim of our study is to investigate the mechanism of metastasis, to detect novel metastasis-associated molecules, and to evaluate the molecules from the point of view of clinical application. A monoclonal antibody MH8-11, which we established, recognizes a glycoprotein that is identical to aminopeptidase N (APN/CD13). APN/CD13 degrades the extracellular matrix, while it is also involved in cell motility and improves angiogenesis. EXPERIMENTAL
DESIGN: We investigated the expression of APN/CD13 in 194 cases of non-small cell lung cancer (NSCLC) by immunohistochemical analyses and reverse transcription-PCR assay to determine the significance of this prognostic factor; 95 tumors were stage I, 36 were stage II, 39 were stage IIIA, and 24 were stage IIIB. Moreover, we investigated that the relationship between the expression of APN/CD13 and angiogenesis and prognosis for patients with NSCLC.
RESULTS: We found a correlation between the expression of APN/CD13 and angiogenesis (r = 0.659; P < 0.0001). In the 194 patients with NSCLC, we found 68 patients to be APN/CD13+ and 126 patients to be APN/CD13-. The 5-year survival rate in patients with APN/CD13+ tumors was significantly lower than in those whose tumors had negative APN/CD13 (48.3% versus 67.1%; P = 0.0001).
CONCLUSION: Our data suggest the expression of APN/CD13 for patients with NSCLC to be associated with a poor prognosis and angiogenesis. This is the first study to show the relationship between the expression of APN/CD13 and the prognosis of patients with NSCLC. The inhibition of APN/CD13 may be an effective new molecular target therapy for patients with NSCLC.

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Year:  2006        PMID: 16818694     DOI: 10.1158/1078-0432.CCR-06-0338

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  34 in total

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Authors:  Gopal Pathuri; Andria F Hedrick; Bryan C Disch; John T Doan; Michael A Ihnat; Vibhudutta Awasthi; Hariprasad Gali
Journal:  Bioconjug Chem       Date:  2011-12-20       Impact factor: 4.774

2.  Cooperative effects of aminopeptidase N (CD13) expressed by nonmalignant and cancer cells within the tumor microenvironment.

Authors:  Liliana Guzman-Rojas; Roberto Rangel; Ahmad Salameh; Julianna K Edwards; Eleonora Dondossola; Yun-Gon Kim; Alan Saghatelian; Ricardo J Giordano; Mikhail G Kolonin; Fernanda I Staquicini; Erkki Koivunen; Richard L Sidman; Wadih Arap; Renata Pasqualini
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-17       Impact factor: 11.205

3.  Quantitative Multiplex Substrate Profiling of Peptidases by Mass Spectrometry.

Authors:  John D Lapek; Zhenze Jiang; Jacob M Wozniak; Elena Arutyunova; Steven C Wang; M Joanne Lemieux; David J Gonzalez; Anthony J O'Donoghue
Journal:  Mol Cell Proteomics       Date:  2019-01-31       Impact factor: 5.911

4.  Prognostic value of matrix metalloproteinase-2 (MMP-2), matrix metalloproteinase-9 (MMP-9) and aminopeptidase N/CD13 in breast cancer patients.

Authors:  Irena Ranogajec; Jasminka Jakić-Razumović; Velibor Puzović; Jelka Gabrilovac
Journal:  Med Oncol       Date:  2011-05-25       Impact factor: 3.064

5.  Enhanced expression of CD13 in vessels of inflammatory and neoplastic tissues.

Authors:  Paola Di Matteo; Gian Luigi Arrigoni; Luca Alberici; Angelo Corti; Corrado Gallo-Stampino; Catia Traversari; Claudio Doglioni; Gian-Paolo Rizzardi
Journal:  J Histochem Cytochem       Date:  2011-01       Impact factor: 2.479

6.  Design, Synthesis, and Biological Evaluation of APN and AKT Dual-Target Inhibitors.

Authors:  Qian Liu; Hang Dong; Wei Zhao; Guozhen Zhang; Shunda Li; Qifu Xu; Yingjie Zhang
Journal:  ACS Med Chem Lett       Date:  2021-11-10       Impact factor: 4.345

7.  Proteolytic cleavage of a C-terminal prosequence, leading to autoprocessing at the N Terminus, activates leucine aminopeptidase from Pseudomonas aeruginosa.

Authors:  Robert Sarnovsky; Jennifer Rea; Matt Makowski; Ralf Hertle; Colleen Kelly; Antonella Antignani; Diana V Pastrana; David J Fitzgerald
Journal:  J Biol Chem       Date:  2009-02-11       Impact factor: 5.157

8.  The novel alkylating prodrug J1: diagnosis directed activity profile ex vivo and combination analyses in vitro.

Authors:  Malin Wickström; Caroline Haglund; Henrik Lindman; Peter Nygren; Rolf Larsson; Joachim Gullbo
Journal:  Invest New Drugs       Date:  2007-10-06       Impact factor: 3.850

9.  Melphalan-flufenamide is cytotoxic and potentiates treatment with chemotherapy and the Src inhibitor dasatinib in urothelial carcinoma.

Authors:  Kristina Viktorsson; Carl-Henrik Shah; Therese Juntti; Petra Hååg; Katarzyna Zielinska-Chomej; Adam Sierakowiak; Karin Holmsten; Jessica Tu; Jack Spira; Lena Kanter; Rolf Lewensohn; Anders Ullén
Journal:  Mol Oncol       Date:  2016-01-02       Impact factor: 6.603

10.  First-in-human, phase I/IIa clinical study of the peptidase potentiated alkylator melflufen administered every three weeks to patients with advanced solid tumor malignancies.

Authors:  Åke Berglund; Anders Ullén; Alla Lisyanskaya; Sergey Orlov; Hans Hagberg; Bengt Tholander; Rolf Lewensohn; Peter Nygren; Jack Spira; Johan Harmenberg; Markus Jerling; Carina Alvfors; Magnus Ringbom; Eva Nordström; Karin Söderlind; Joachim Gullbo
Journal:  Invest New Drugs       Date:  2015-11-10       Impact factor: 3.850

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