Department Chair
Email: [email protected]
Location: Cleveland Clinic Main Campus
The Bowler Lab seeks to understand how smoke inhalation from cigarettes and e-cigarettes/vapes (tobacco and cannabis) causes chronic obstructive pulmonary disease (COPD), the third leading cause of death in the United States.
Because the widespread, legal use of marijuana and e-cigarettes/vapes is so new, the effects of these types of inhaled smokes on our lungs are not fully understood. Similarly, while the effects of tobacco smoke and cigarettes on our lungs are well known, the biological processes causing these effects are not. Understanding the “whats,” “hows,” and “whys” behind smoke inhalation risks is necessary to help people make informed decisions about their health and habits.
Our lab employs a combination of computational and experimental techniques to achieve our goals.
Russell Bowler, MD, PhD, is a practicing physician-scientist with over 25 years of experience as a pulmonologist and researcher. He is trained in mathematical and computational sciences, cell and developmental biology, internal medicine and pulmonary critical care. Dr. Bowler built his research program on learning about how biological and environmental factors influence someone's risk of developing lung diseases.
Dr. Bowler is one of the highest-cited proteomics experts in the world and has published over 300 manuscripts. His research is supported by federally funded grants and industry contracts and has led to multiple patents. He is a leader of genetics, proteomics and multi-omics in the NIH TransOmic Precision Medicine Program.
Prior to joining Cleveland Clinic, Dr. Bowler was director of the Precision Medicine Program at National Jewish Health in Colorado.
Education
Professional Highlights
The Bowler lab integrates high-throughput genomic, proteomic, and metabolic data from population-based studies (COPDGene and SPIROMICS) to understand the molecular mechanisms of how inhaled tobacco and cannabis smoke (cigarette and e-cig/vape) causes COPD. We seek to identify diagnostic and therapeutic biomarkers that contribute to:
We have many ongoing in vitro, in vivo and in silico projects.
Recent technical advances in multi-omic platforms (genetics, genomics, proteomics, metabolomics, etc.) allow us to conduct high-throughput, large scale investigations into the molecular basis of complex lung diseases like COPD and emphysema. We have created a 2000 subject cohort of current and former smokers with and without COPD and emphysema within the NIH sponsored COPDGene® cohort.
In recently published pilot studies, we have shown that we integrated and leveraged these multi-omic studies to identify novel molecular pathways that appear to be deranged in certain patients with COPD and emphysema. Examples of these pathways include ceramide/sphingolipid and Arghef1 signaling.
We have developed preclinical models to study the interplay between genetics and environmental factors in COPD. We use gene knock-outs to examine the effects of cigarette smoke inhalation in relation to COPD and emphysema. We seek to inhibit metabolic targets identified in our multi-omic patient analyses, to in turn inhibit key pathogenic mechanisms of smoke-induced lung disease.
In preclinical models we have found molecular therapies that specifically target pathways identified in our multi-omic integrations (e.g. sphingosine 1-phosphate analogues and thromboxane antagonists respectively) and can reverse some of the COPD and emphysema-like changes caused by cigarette smoke.
We seek to leverage data from larger, more diverse population studies of COPD and emphysema patients to identify more pathways that can be targeted for drug development. We are currently following up on multiple inflammation-related genes to achieve our goals.
We have ongoing studies investigating the effects of vaping on individuals aged 18-25. Efforts to establish a study cohort in Northeast Ohio are ongoing.
View publications for Russell P. Bowler, MD, PhD
(Disclaimer: This search is powered by PubMed, a service of the U.S. National Library of Medicine. PubMed is a third-party website with no affiliation with Cleveland Clinic.)
Bowler Russell P. Dynamic and prognostic proteomic associations with FEV decline in chronic obstructive pulmonary disease. medRxiv. 2024. 39148837.
Erzurum Serpil C, Zein Joe. Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium. Genome Med. 2021. 33883027.
Lowe Katherine E. COPDGene 2019: Redefining the Diagnosis of Chronic Obstructive Pulmonary Disease. Chronic Obstr Pulm Dis. 2019. 31710793.
Dr. Bowler has mentored over 30 trainees, including students and postdoctoral researchers. He is strongly committed to nurturing the future generation of researchers, physicians, critical thinkers and leaders. Specific job postings are listed below, but all interested applicants are encouraged to reach out.
In the Bowler Lab, we love what we do! We chase the thrill of discovery, and we are proud of our contributions to improving one of the most prevalent public health issues facing our generation. We’re looking for people who feel the same; the Bowler lab is seeking driven postdoctoral, graduate and undergraduate researchers! Please send a CV and a letter of interest to [email protected] and [email protected].
Postdoctoral applicants must be comfortable with standard wet lab techniques, comfortable working with murine models, and have a background in pulmonary/lung-related research.
It is suggested that student applicants be comfortable with/have a background in coding and computational work, though all are welcome to apply!
Our education and training programs offer hands-on experience at one of the nationʼs top hospitals. Travel, publish in high impact journals and collaborate with investigators to solve real-world biomedical research questions.
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