Public Release:  Novel blood-based protein signature determined for rare, aggressive lung cancer

Identified biomarkers may enable early diagnosis of malignant mesothelioma, a cancer linked to prolonged asbestos exposure

PLOS

Researchers have discovered a panel of 13 blood proteins that may be effective biomarkers to detect malignant mesothelioma, according to a study published Oct. 3 in the open access journal PLOS ONE by Rachel Ostroff from the company SomaLogic, which developed the new test, and colleagues at other institutions.

Malignant mesothelioma is a rare, aggressive form of lung cancer that can develop after prolonged exposure to asbestos. Because early diagnosis is difficult, most patients face a poor prognosis and have few options for treatment. In the study, authors compared proteins in the blood of asbestos-exposed individuals without the disease to blood proteins in asbestos-exposed mesothelioma patients to identify 13 proteins that are linked to the disease, including in the early stages.

According to the researchers, the discovery of the new blood-based proteins linked to the disease could help to develop better, less invasive diagnostic tests to detect the disease at earlier stages.

"By measuring changes in blood concentration of a series of proteins we can potentially catch mesothelioma at an earlier stage," said Ostroff, Clinical Research Director at SomaLogic. "Our efforts are now focused on further development of this approach, and how best to get it rapidly into clinical use for the sake of individuals who can benefit from earlier detection of this devastating disease."

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Citation: Ostroff RM, Mehan MR, Stewart A, Ayers D, Brody EN, et al. (2012) Early Detection of Malignant Pleural Mesothelioma in Asbestos-Exposed Individuals with a Noninvasive Proteomics-Based Surveillance Tool. PLoS ONE 7(10): e46091. doi:10.1371/journal.pone.0046091

Financial Disclosure: SomaLogic funded the proteomic analyses. Funding for all other aspects of the study including cohort assembly and ELISA completion was through National Cancer Institute Early Detection Research Grant 2U01CA111295-04 to HIP. SomaLogic had a role in the study design, data collection and analysis, decision to publish, and preparation of the manuscript.

Competing Interest Statement: We have read the journal's policy and have the following conflicts: RO, MM, AS, DA, EB, and SW are employees of SomaLogic. SomaLogic funded the proteomic analyses. This does not alter our adherence to all the PLoS ONE policies on sharing data and materials. The remaining authors have no conflict of interest.

PLEASE LINK TO THE SCIENTIFIC ARTICLE IN ONLINE VERSIONS OF YOUR REPORT (URL goes live after the embargo ends): http://dx.plos.org/10.1371/journal.pone.0046091

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