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Christine M. Lovly | |
|---|---|
| Alma mater | Johns Hopkins University (BSc) Washington University in St. Louis (MS, PhD) |
| Scientific career | |
| Institutions | Vanderbilt University |
Christine M. Lovly is an Associate Professor of Medicine at Vanderbilt University. Her research involves the development of novel treatment strategies for ALK positive lung cancer.
Early life and education
Lovly realised that she wanted to help people suffering from cancer at the age of sixteen.[1] She studied chemistry at Johns Hopkins University.[2] She moved to Washington University in St. Louis for her graduate studies, where she joined the medical scientist training programme. She earned an MD–PhD in 2006. Lovly trained in internal medicine and medical oncology at Vanderbilt University and completed her residency in 2008. She was board certified in 2012 by the American Board of Internal Medicine.[3]
Research and career
In 2012 Lovly joined the faculty at Vanderbilt University, where she serves as Associate Professor and Co-Leader, Translational Research and Interventional Oncology Program at Vanderbilt University Medical Center.[2][4] Her research focusses on understanding and developing novel therapeutic strategies for molecular subsets of lung cancer. In the United States, lung cancer is responsible for more death than any other form of cancer. Her research involves the development of combination therapies that are able to target cancers with abnormal cellular pathways.[1] Lovly has identified particular mutations that can contribute to a person becoming resistant to therapy.[1]
Advanced metastatic disease, cancer which has spread from where it started in the lung, has historically been treated using chemotherapy.[5] Some lung cancer patients have molecular alterations that can permit targeted treatments.[5] Some of these include alterations in the protein Anaplastic Lymphoma Kinase (ALK) receptor tyrosine kinase.[5][6] When this protein is altered, there is potential for pharmaceuticals that block the action of the mutant ALK gene, but almost all patients develop resistance to them.[5][7]
It is known that non-small-cell lung carcinoma (NSCLC) do not respond as effectively to combination drugs as other forms of lung cancer.[8] Lovly has worked with computer scientists to develop algorithms that can identify the drug interactions that are effective at killing tumours and result in fewer side effects.[9][10] Lovly has investigated TAK-788 as a targeted therapy for people with NSCLC and BLU-667 for patients with RET rearrangements.[11][12]
She is involved with the Vanderbilt University online resource My Cancer Genome, which contains information about cancer mutations and the impact they may have on the treatment of patients with cancer.[13] She is supported by the American Society of Clinical Oncology and the Lung Cancer Foundation of America.[14][15]
Selected publications
Her publications include:
- Lovly, Christine (2012-03-10). "ROS1 rearrangements define a unique molecular class of lung cancers". Journal of Clinical Oncology. 30: 863. doi:10.1200/JCO.2011.35.6345.
- Lovly, Christine (2001). "Localization of human Cdc25C is regulated both by nuclear export and 14-3-3 protein binding". Oncogene. 20: 1839. doi:10.1038/sj.onc.1204259.
- Lovly, Christine (2012-04-20). "Routine multiplex mutational profiling of melanomas enables enrollment in genotype-driven therapeutic trials". PloS one. 7. doi:10.1371/journal.pone.0035309.
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References
- ^ a b c "Celebrate Women's History Month: Christine M. Lovly, Targeting Lung Cancer". Damon Runyon. Retrieved 2020-01-15.
- ^ a b "Lovly [1571] | Vanderbilt-Ingram Cancer Center". www.vicc.org. Retrieved 2020-01-15.
- ^ "Christine M. Lovly, MD, PhD, BA | Vanderbilt Health Nashville, TN". search.vanderbilthealth.com. Retrieved 2020-01-16.
- ^ admin. "Q&A With Lung Cancer Specialist Dr. Christine Lovly | T.J. Martell Foundation Blog". Retrieved 2020-01-16.
- ^ a b c d "Meet Our Scientists". Damon Runyon. Retrieved 2020-01-15.
- ^ "Vanderbilt Oncologists Publish Results of First Study to Demonstrate Clinical Utility of Resolution Liquid Biopsy Assay to Monitor Response and Resistance to Ensartinib". www.businesswire.com. 2019-10-29. Retrieved 2020-01-16.
- ^ "PHYSICIAN SPOTLIGHT: Dr. Christine Lovly Gains Worldwide Renown in Cancer Research". Nashville Medical News. 2014-09-04. Retrieved 2020-01-16.
- ^ "RET Rearrangements in Non-Small Cell Lung Cancer". Targeted Oncology. Retrieved 2020-01-16.
- ^ Hall, Heidi. "New algorithm calculates drug synergy; initial tests involve melanoma, lung cancer". Vanderbilt University. Retrieved 2020-01-16.
- ^ "'Mind-boggling' IO Data, Plus New Combos, Targets for NSCLC". Medscape. Retrieved 2020-01-16.
- ^ "Two New Targeted Therapies Appear Encouraging for Difficult Drivers in NSCLC". Targeted Oncology. Retrieved 2020-01-16.
- ^ "New Therapies Intriguing for Elusive Targets in NSCLC". OncLive. Retrieved 2020-01-16.
- ^ "PHYSICIAN SPOTLIGHT: Dr. Christine Lovly Gains Worldwide Renown in Cancer Research". Nashville Medical News. 2014-09-04. Retrieved 2020-01-16.
- ^ "Christine Lovly, Lung Cancer Foundation of America Class of 2017". Lung Cancer Foundation of America. Retrieved 2020-01-16.
- ^ "The American Society for Clinical Investigation". Retrieved 2020-01-16.