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US 11,634,778 B2Granted
Kit, device, and method for detecting lung cancer
AssigneesToray Industries, Inc., National Cancer Center
InventorsYuho Kida, Satoko Kozono, Hiroko Sudo, Satoshi Kondou, Junpei Kawauchi, Takahiro Ochiya, Shun-Ichi Watanabe
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Abstract
This application provides a kit or a device for detection of lung cancer, comprising a nucleic acid(s) for detecting a miRNA(s) in a sample from a subject, and a method for detecting lung cancer, comprising measuring the miRNA(s) in vitro.
Claims7
A method for detecting and treating or performing a diagnostic procedure for lung cancer, comprising:
- determining an expression level of hsa-miR-2467-3p in a sample from a human subject using a nucleic acid(s) capable of specifically binding to hsa-miR-2467-3p, or using a kit or device comprising a nucleic acid(s) capable of specifically binding to hsa-miR-2467-3p,
- wherein the determining comprises the following steps of:
- (a) contacting hsa-miR-2467-3p in the sample or complementary polynucleotide(s) thereof prepared from hsa-miR-2467-3p with the nucleic acid(s);
- (b) measuring an expression level of hsa-miR-2467-3p;
- (c) comparing the expression level of hsa-miR-2467-3p measured in the step (b) to a control expression level of hsa-miR-2467-3p in a control sample from a healthy human subject measured in the same way as in the step (b) to allow for diagnosis of lung cancer;
- (d) detecting an increased level of hsa-miR-2467-3p in the sample from the human subject as compared to the control expression level of hsa-miR-2467-3p from the sample from the human subject that does not have lung cancer, wherein the increased level of hsa-miR-2467-3p indicates that the human subject has lung cancer;
- and
- (e) treating the human subject having lung cancer or performing a diagnostic procedure on the human subject having lung cancer;
- wherein the sample is blood, serum, or plasma;
- wherein the treatment comprises chemotherapy, radiotherapy, immunotherapy, molecular targeted therapy, surgery or a combination thereof;
- and
- wherein the diagnostic procedure comprises an imaging test method selected from the group consisting of a chest X-ray examination, CT examination, MRI examination, and PET examination;
- a pathological examination method selected from the group consisting of sputum cytology, pleural fluid analysis, bronchoscopy, and percutaneous needle biopsy;
- or a combination thereof.
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Dependencies are inferred from the claim text.