CPC G01N 33/57423 (2013.01) [A61K 39/3955 (2013.01); A61K 39/39558 (2013.01); A61K 45/06 (2013.01); A61P 35/00 (2018.01); C07K 16/22 (2013.01); C07K 16/26 (2013.01); C07K 16/3023 (2013.01); C07K 16/32 (2013.01); C07K 2317/22 (2013.01); C07K 2317/24 (2013.01); C07K 2317/34 (2013.01); C07K 2317/51 (2013.01); C07K 2317/515 (2013.01); C07K 2317/565 (2013.01); C07K 2317/569 (2013.01); C07K 2317/76 (2013.01); G01N 2333/595 (2013.01)] | 20 Claims |
1. A method for the in vitro diagnosis of lung cancer in a subject, said method comprising:
a) obtaining a biological sample from said subject,
b) detecting whether progastrin is present in said biological sample by contacting said biological sample with at least one progastrin-binding molecule, wherein said progastrin-binding molecule is a monoclonal antibody produced by the hybridoma deposited at the CNCM, Institut Pasteur, 25-28 rue du Docteur Roux, 75724 Paris CEDEX 15, France, on 27 Dec. 2016, under reference 1-5158,
c) detecting the binding of said progastrin-binding molecule to progastrin in said biological sample,
d) detecting whether a lung cancer biomarker is present in said biological sample, and
e) diagnosing said subject with a lung cancer when the presence of progastrin and said lung cancer biomarker is detected.
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