1. The Cancer Prevention Project of Philadelphia: preliminary findings examining diversity among the African diaspora
- Author
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Vera Tolbert, Carlene Bowen, Robin Roberts, Meganathan P. Ramakodi, Yin-Ming Kuo, Daramola N Cabral, Camille Ragin, JoAnn S. Oliver, Andrew J. Andrews, Gilda Jean-Louis, Barbara Wilson, Elizabeth Blackman, Raphiatou Noumbissi, Oni Richards-Waritay, Eric Edi, Karthik Devarajan, Kimlin Tam Ashing, Jackie Bucci, Marshall K. Tulloch-Reid, and Denise Gibbs
- Subjects
Cultural Studies ,Gerontology ,Human Migration ,media_common.quotation_subject ,Afro-Caribbean ,Article ,Diaspora ,03 medical and health sciences ,0302 clinical medicine ,Arts and Humanities (miscellaneous) ,Neoplasms ,Health care ,Cancer screening ,Ethnicity ,Humans ,030212 general & internal medicine ,Sociology ,media_common ,Philadelphia ,Cancer mortality ,Smokers ,030505 public health ,Cancer prevention ,business.industry ,Public Health, Environmental and Occupational Health ,0305 other medical science ,business ,Inclusion (education) ,Diversity (politics) - Abstract
OBJECTIVE: Cancer mortality inequity among persons of African Ancestry is remarkable. Yet, Black inclusion in cancer biology research is sorely lacking and warrants urgent attention. Epidemiologic research linking African Ancestry and the African Diaspora to disease susceptibility and outcomes is critical for understanding the significant and troubling health disparities among Blacks. Therefore, in a cohort of diverse Blacks, this study examined differences in genetic ancestry informative markers (AIMs) in the DNA repair pathway and the cancer related biomarker 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL). METHODS: Participants completed a questionnaire and provided bio-specimens. AIMs in or around DNA repair pathway genes were analyzed to assess differences in minor allele frequency (MAF) across the 3 ethnic subgroups. NNAL concentration in urine was measured among current smokers. RESULTS: To date the cohort includes 852 participants, 88.3% being Black. Of the 752 Blacks, 51.3% were US-born, 27.8% were Caribbean-born, and 19.6% were Africa-born. Current and former smokers represented 14.9% and 10.0%, respectively. US-born Blacks were more likely to be smokers and poor metabolizers of NNAL. Two-way hierarchical clustering revealed MAF of AIMs differed across the 3 ethnic subgroups. CONCLUSION: Our findings are consistent with the emerging literature demonstrating Black heterogeneity underscoring African Ancestry genetic subgroup differences— specifically relevant to cancer. Further investigations, with data harmonization and sharing, are urgently needed to begin to map African Ancestry cancer biomarkers as well as race, and race by place\region comparative biomarkers to inform cancer prevention and treatment in the era of precision medicine.
- Published
- 2018