Sparse Supervised Classification Methods Predict and Characterize Nanomaterial Exposures: Independent Markers of MWCNT Exposures. (January 2018)

• Record Type: Journal Article
• Authors: Yanamala, Naveena; Orandle, Marlene S.; Kodali, Vamsi K.; Bishop, Lindsey; Zeidler-Erdely, Patti C.; Roberts, Jenny R.; Castranova, Vincent; Erdely, Aaron
• Other Names: Hubbs Ann guest-editor.; Monteiro-Riviere Nancy guest-editor.; Orandle Marlene guest-editor.
• Is Part Of: Toxicologic pathology. Volume 46:Number 1(2018)
• Page Start: 14
• Page End: 27
• Publication Date: 2018-01
• Subjects: fibrosis markers -- computational toxicology -- nanotoxicology -- predictive models -- support vector machines; Pathology -- Periodicals; Toxicology -- Periodicals; Pathology; Toxicology; 615.9
• DOI: 10.1177/0192623317730575
• Languages: English
• ISSNs: 0192-6233

Abstract

Recent experimental evidence indicates significant pulmonary toxicity of multiwalled carbon nanotubes (MWCNTs), such as inflammation, interstitial fibrosis, granuloma formation, and carcinogenicity. Although numerous studies explored the adverse potential of various CNTs, their comparability is often limited. This is due to differences in administered dose, physicochemical characteristics, exposure methods, and end points monitored. Here, we addressed the problem through sparse classification method, a supervised machine learning approach that can reduce the noise contained in redundant variables for discriminating among MWCNT-exposed and MWCNT-unexposed groups. A panel of proteins measured from bronchoalveolar lavage fluid (BAL) samples was used to predict exposure to various MWCNT and determine markers that are attributable to MWCNT exposure and toxicity in mice. Using sparse support vector machine–based classification technique, we identified a small subset of proteins clearly distinguishing each exposure. Macrophage-derived chemokine (MDC/CCL22), in particular, was associated with various MWCNT exposures and was independent of exposure method employed, that is, oropharyngeal aspiration versus inhalation exposure. Sustained expression of some of the selected protein markers identified also suggests their potential role in MWCNT-induced toxicity and proposes hypotheses for future mechanistic studies. Such approaches can be used more broadly for nanomaterial risk profiling studies to evaluate decisions related to dose/time–response relationships that could delineate experimental variables from exposure markers.