Proteomic patterns of tumour subsets in non-small-cell lung cancer

Kiyoshi Yanagisawa, Yu Shyr, Baogang J. Xu, Pierre P. Massion, Paul H. Larsen, Bill C. White, John R. Roberts, Mary Edgerton, Adriana Gonzalez, Sorena Nadaf, Jason H. Moore, Richard M. Caprioli, David P. Carbone

Research output: Contribution to journalArticlepeer-review

529 Citations (Scopus)


Background: Proteomics-based approaches complement the genome initiatives and may be the next step in attempts to understand the biology of cancer. We used matrix-assisted laser desorption/ionisation mass spectrometry directly from 1-mm regions of single frozen tissue sections for profiling of protein expression from surgically resected tissues to classify lung tumours. Methods: Proteomic spectra were obtained and aligned from 79 lung tumours and 14 normal lung tissues. We built a class-prediction model with the proteomic patterns in a training cohort of 42 lung tumours and eight normal lung samples, and assessed their statistical significance. We then applied this model to a blinded test cohort, including 37 lung tumours and six normal lung samples, to estimate the misclassification rate. Findings: We obtained more than 1600 protein peaks from histologically selected 1 mm diameter regions of single frozen sections from each tissue. Class-prediction models based on differentially expressed peaks enabled us to perfectly classify lung cancer histologies, distinguish primary tumours from metastases to the lung from other sites, and classify nodal involvement with 85% accuracy in the training cohort. This model nearly perfectly classified samples in the independent blinded test cohort. We also obtained a proteomic pattern comprised of 15 distinct mass spectrometry peaks that distinguished between patients with resected non-small-cell lung cancer who had poor prognosis (median survival 6 months, n=25) and those who had good prognosis (median survival 33 months, n=41, p<0.0001). Interpretation: Proteomic patterns obtained directly from small amounts of fresh frozen lung-tumour tissue could be used to accurately classify and predict histological groups as well as nodal involvement and survival in resected non-small-cell lung cancer.

Original languageEnglish
Pages (from-to)433-439
Number of pages7
Issue number9382
Publication statusPublished - 2003 Aug 9

All Science Journal Classification (ASJC) codes

  • Medicine(all)


Dive into the research topics of 'Proteomic patterns of tumour subsets in non-small-cell lung cancer'. Together they form a unique fingerprint.

Cite this