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  • 1
    Online Resource
    Online Resource
    Elsevier BV ; 2021
    In:  Ecotoxicology and Environmental Safety Vol. 219 ( 2021-08), p. 112327-
    In: Ecotoxicology and Environmental Safety, Elsevier BV, Vol. 219 ( 2021-08), p. 112327-
    Type of Medium: Online Resource
    ISSN: 0147-6513
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2021
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    SSG: 24,1
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2023
    In:  Cancer Epidemiology, Biomarkers & Prevention Vol. 32, No. 12_Supplement ( 2023-12-01), p. B096-B096
    In: Cancer Epidemiology, Biomarkers & Prevention, American Association for Cancer Research (AACR), Vol. 32, No. 12_Supplement ( 2023-12-01), p. B096-B096
    Abstract: Background: Smoking is a modifiable lifestyle factor linked to prostate cancer (PCa) risk, but its association with PCa aggressiveness is unclear. Further, African-American men are likelier to smoke and be at risk for PCa. Therefore, we examined racial disparities in the association between cigarette smoking and PCa aggressiveness. Methods: Data for this study came from the North Carolina-Louisiana Prostate Cancer Project, a registry-based cohort study of incident PCa cases from 2004-2009 (n = 1,457). We defined PCa aggressiveness as high (Gleason score ≥ 8, Gleason score = 7 and TNM T3-T4, or prostate-specific antigen (PSA) score & gt; 20 ng/mL) or low (Gleason score & lt; 7, TNM T1-T2, and PSA & lt; 10 ng/mL). We classified cigarette smoking as current, former, or never. Our analyses used multivariable logistic regression to estimate adjusted odds ratios (OR) and 95% confidence intervals (CI). Results: One-third (35%) of PCa cases were high-aggressive. Half (48%) of the study sample was African-American. Current smoking, but not former smoking, was associated with high-aggressive PCa compared to never (OR = 2.2; 95% CI [1.5, 3.3]). African-Americans who currently smoked had higher odds of high-aggressive PCa than those who never smoked (OR = 3.2; 95% CI [1.9, 5.4] ), as did those who formerly smoked (OR = 1.8; 95% CI [1.2, 2.3]). However, smoking did not significantly predict PCa aggressiveness in European-Americans. Conclusion: Cigarette smoking is associated with PCa aggressiveness, an association moderated by race. Future research should investigate the biological and social effects of smoking and PCa aggressiveness between racial groups.  Citation Format: Edgar T. Ellis, Brian J. Fairman, Shelbie D. Stahr, L. Joseph Su, Ping-Ching Hsu. Cigarette smoking and prostate cancer aggressiveness among African and European American men [abstract]. In: Proceedings of the 16th AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2023 Sep 29-Oct 2;Orlando, FL. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2023;32(12 Suppl):Abstract nr B096.
    Type of Medium: Online Resource
    ISSN: 1538-7755
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2023
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  • 3
    In: JMIR Formative Research, JMIR Publications Inc., Vol. 6, No. 1 ( 2022-1-10), p. e19750-
    Abstract: Obesity is significantly associated with renal cell carcinoma. Surgery is the preferred treatment for demarcated lesions of renal cell carcinoma; however, obesity increases the complexity of surgical outcomes. Minimally invasive surgical techniques are preferred over open partial nephrectomy (OPN), but controversy remains regarding the most efficacious technique in patients with obesity. Objective This study aims to determine whether minimally invasive partial nephrectomy (MIPN) or OPN better preserves renal function and investigate short- and long-term renal outcomes in patients with obesity undergoing a partial nephrectomy. Methods We conducted a retrospective chart review of 242 adult patients aged ≥18 years who underwent MIPN or OPN between January 1, 2005, and December 31, 2016, at the University of Arkansas for Medical Sciences. Using creatinine as a measure of kidney function, patients’ preoperative levels were compared with their postoperative levels in 2-time frames: short (3-6 months postsurgery) or long ( 〉 6 months). The primary outcome was the change in creatinine values from preoperative to 〉 6 months postoperatively in patients with obesity. Secondary outcomes included the change in creatinine values from preoperative to 3 to 6 months postoperatively in patients with obesity who underwent MIPN versus OPN. We also analyzed the creatinine values of nonobese patients (BMI 〈 30) who underwent partial nephrectomy using the same time frames. Unconditional logistic regression was used to estimate crude and multivariable-adjusted odds ratios (ORs) and 95% CI to observe associations between surgery type and changes in creatinine values from while stratifying for obesity. Results A total of 140 patients were included in the study, of whom 75 were obese and 65 were nonobese. At 〉 6 months after MIPN (n=20), the odds of patients with obesity having a decrease or no change in creatinine values was 1.24 times higher than those who had OPN (n=13; OR 1.24, 95% CI 0.299-6.729; P=.80). At 3 to 6 months after MIPN (n=27), the odds were 0.62 times lower than those after OPN (n=17; OR 0.62, 95% CI 0.140-2.753; P=.56). In the nonobese group, at 3 to 6 months after undergoing minimally invasive surgery (n=18), the odds of having a decrease or no change in creatinine values was 4.86 times higher than those who had open surgery (n=21; OR 4.86, 95% CI 1.085-21.809; P=.04). At more than 6 months after MIPN (n=14), the odds were 4.13 times higher than those after OPN (n=11; OR 4.13, 95% CI 0.579-29.485; P=.16). Conclusions We observed a nonstatistically significant preservation of renal function in patients with obesity who underwent OPN at 3 to 6 months postoperatively. Conversely, after 6 months, the same was true for MIPN, indicating the long-term benefit of MIPN. In the nonobese group, MIPN was favored over OPN. 
    Type of Medium: Online Resource
    ISSN: 2561-326X
    Language: English
    Publisher: JMIR Publications Inc.
    Publication Date: 2022
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  • 4
    In: Exposure and Health, Springer Science and Business Media LLC, Vol. 13, No. 2 ( 2021-06), p. 269-280
    Abstract: Both arsenic and cadmium are reported to be toxic to humans. The use of saliva as a biomarker of low-level exposures to these elements has not been adequately explored, and the putative relationship between exposure and obesity is unclear. This cross-sectional study aims to investigate the relationship between salivary arsenic and cadmium concentrations and their association with obesity. Arsenic and cadmium concentrations were analyzed in human saliva samples by Inductively Coupled Plasma-Mass Spectrometry on 270 randomly selected women who participated in the Arkansas Rural Community Health Study. Multivariable logistic regression was performed to evaluate the association between heavy metal concentrations and obesity. Stratified logistic regression was performed based on menopausal status. Generalized linear models were used to evaluate weight gain velocity. Significant positive associations were observed in postmenopausal women for both arsenic (OR = 4.43, 95% CI 1.91–10.28) and cadmium (OR = 2.72, 95% CI 1.23–5.99) concentrations, as well as significant trends among tertiles ( p   〈  0.01 and p  = 0.01, respectively). No relationship with obesity was evident among premenopausal women for either metal. A dose–response relationship was observed between increasing weight gain velocity and increasing metal concentrations. At concentrations well below governmental and industrial standards for acute toxicity, significant associations between obesity and concentration of these heavy metals are evident. The rate at which individuals gain weight is affected by metal concentrations and may play a role in the rapid increase in weight in postmenopausal women. These results might explain, in part, the missing variability in the increasing obesity pandemic in certain population exposed to these environmental toxicants.
    Type of Medium: Online Resource
    ISSN: 2451-9766 , 2451-9685
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
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  • 5
    Online Resource
    Online Resource
    AME Publishing Company ; 2019
    In:  Translational Cancer Research Vol. 8, No. S4 ( 2019-7), p. S366-S377
    In: Translational Cancer Research, AME Publishing Company, Vol. 8, No. S4 ( 2019-7), p. S366-S377
    Type of Medium: Online Resource
    ISSN: 2218-676X , 2219-6803
    Language: Unknown
    Publisher: AME Publishing Company
    Publication Date: 2019
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  • 6
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2022
    In:  Cancer Research Vol. 82, No. 12_Supplement ( 2022-06-15), p. 1450-1450
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 82, No. 12_Supplement ( 2022-06-15), p. 1450-1450
    Abstract: Background: DNA methyltransferases (DNMTs) control DNA methylation and impact gene expression. Many studies have demonstrated that genetic variants in DNMT genes play a role in cancer development, including breast cancer. However, the impact of SNP-SNP interactions for DNMTs associated with breast cancer risk is unclear. The objective is to evaluate SNP-SNP interactions associated with breast cancer risk. Methods: We selected 14 SNPs in 3 DNMT genes (DNMT1, DNMT3A, and DNMT3B) for the 4,195 women (1:2 match for breast cancer cases and controls), including 1,085 African Americans (AAs) and 3,110 European Americans (EAs) in the Arkansas Rural Community Health (ARCH) cohort. We included different inheritance models (dominant, recessive, and additive) for individual SNP effects, using logistic regressions with breast cancer status (yes/no) as the outcome. Two-way SNP-SNP interactions associated with breast cancer risk were analyzed using the SNP Interaction Pattern Identifier (SIPI) approach developed by our research team. Results: Out of the 14 DNMTs SNPs, we found two SNPs (rs7605753 and rs10196635 in DNMT3A) were individually associated with breast cancer risk (p & lt;0.05) in EAs, however, none was statistically significant in AAs. Interestingly, we applied the SIPI approach, targeting SNP-SNP interactions,19 SNP-SNP interaction pairs for EAs, and 6 pairs for AAs associated with breast cancer risk. These promising SNP interaction pairs had an interaction p-value less than 0.05, far less than the p-values of the 2 constituent SNPs. Also, these promising SNP-SNP interaction pairs are different between races. For example, the EA women with the CC + AT/TT genotype in rs12991495 + rs10196635 (both in DNMT3A) had a higher risk of breast cancer risk than other genotype combinations (Odds ratio [OR]=2.2, p=0.011). On the other hand, the AA women with the TT+AA genotype in the SNP pair of rs2304429 (DNMT3A) + rs2290684 (DNMT1) tend to have a higher breast cancer risk than other genotype combinations in the same pair (OR=4.3, p=0.034). Notably, the individual effects of the two constituent SNPs are not significant (p=0.537 and 0.547). Conclusion: Our findings support that the SNPs in DNMT genes play an essential role in breast cancer risk. SIPI is an excellent tool to evaluate SNP-SNP interactions, which can better predict breast cancer risk. Citation Format: Hui-Yi Lin, L. Joseph Su, Lora J. Rogers, Gail A. Runnells, Ping-Ching Hsu, Shelbie D. Stahr, Tung-Chin Chiang. Interactions of DNMTs genetic variants associated with breast cancer risk [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 1450.
    Type of Medium: Online Resource
    ISSN: 1538-7445
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2022
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    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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  • 7
    Online Resource
    Online Resource
    AME Publishing Company ; 2016
    In:  Translational Cancer Research Vol. 5, No. S5 ( 2016-10), p. S944-S950
    In: Translational Cancer Research, AME Publishing Company, Vol. 5, No. S5 ( 2016-10), p. S944-S950
    Type of Medium: Online Resource
    ISSN: 2218-676X , 2219-6803
    Language: Unknown
    Publisher: AME Publishing Company
    Publication Date: 2016
    detail.hit.zdb_id: 2901601-0
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  • 8
    In: International Journal of Radiation Biology, Informa UK Limited, Vol. 99, No. 4 ( 2023-04-03), p. 644-655
    Type of Medium: Online Resource
    ISSN: 0955-3002 , 1362-3095
    RVK:
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2023
    detail.hit.zdb_id: 1498203-1
    SSG: 12
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  • 9
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2020
    In:  Cancer Epidemiology, Biomarkers & Prevention Vol. 29, No. 6_Supplement_1 ( 2020-06-01), p. C049-C049
    In: Cancer Epidemiology, Biomarkers & Prevention, American Association for Cancer Research (AACR), Vol. 29, No. 6_Supplement_1 ( 2020-06-01), p. C049-C049
    Abstract: Background: Although the relationship between physical activity and breast cancer is well established, research demonstrating levels of physical activity and breast cancer association among different racial groups is less definitive. It is perceived by the public that beneficial effects of physical activity depend on the rigorousness of activity performed, and within these levels of physical activity, racial differences are observed. Objectives: The aim of this study is to evaluate levels of physical activity among different racial groups, while stratifying for menopause status, and their relationship to breast cancer. Specifically examining incidence and prevalent breast cancer cases, this study examined potential variation of physical activity in relation to time of cancer diagnosis among different racial groups. Methods: A cohort of 26,387 women in the Arkansas Rural Community Health Study (ARCH) was used to evaluate physical activity and its association with breast cancer among different racial groups. Multiple logistic regression (OR, 95%CI) was used to examine the association between breast cancer and intensity, length, and frequency of physical activity while adjusting for confounding variables, such as age and parity. Demographic and weekly physical activity information was reported at baseline. A Metabolic Equivalent of Task score was derived from the self-reported questionnaire data. Results: A total of 1,455 participants were excluded due to insufficient information regarding breast cancer status, race, and menopausal status, resulting in a sample of 23,980 participants. The analysis consisted of 155 newly diagnosed breast cancer cases after the baseline (incident), 2,330 existing breast cancer cases when entering the study (prevalent), and 21,495 noncancer subjects, of whom 78% identified as European American (EA) and 22% identified as African American (AA). Approximately 49% of eligible participants reported being postmenopausal and 51% being premenopausal. A significant downward trend was observed in vigorous physical activity among EA women for incident and prevalent breast cancer (p= 0.002 and 0.04), whereas no clear trend was seen among AA women due to small sample size. Similar trends can be seen in vigorous physical activity postmenopausal EA women (p= 0.005 and 0.002). The beneficial association was not observed among AA women. On the other hand, overall physical activity appears to be positively associated with breast cancer among AA women (p for trend = 0.04). Conclusions: There appears to be a beneficial effect of vigorous physical activity and breast cancer among EA, regardless of pre- or postmenopausal status. However, the effect does not seem to apply to AA women, which could be the result of small number of breast cancer cases in African Americans. The current physical activity recommendations may not be applicable to all racial groups. We may be able to get a better race-specific recommendation regarding the level of leisure physical activity by pooling our data with other studies. Citation Format: Shelbie Stahr, Gail Runnells, Lora Rogers, Pearl Mcelfish, Susan Kadlubar, Joseph L. Su. The association between breast cancer and physical activity levels by race in a prospective cohort study [abstract]. In: Proceedings of the Eleventh AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2018 Nov 2-5; New Orleans, LA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2020;29(6 Suppl):Abstract nr C049.
    Type of Medium: Online Resource
    ISSN: 1055-9965 , 1538-7755
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2020
    detail.hit.zdb_id: 2036781-8
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  • 10
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2020
    In:  Cancer Epidemiology, Biomarkers & Prevention Vol. 29, No. 12_Supplement ( 2020-12-01), p. PO-201-PO-201
    In: Cancer Epidemiology, Biomarkers & Prevention, American Association for Cancer Research (AACR), Vol. 29, No. 12_Supplement ( 2020-12-01), p. PO-201-PO-201
    Abstract: Background. Significant racial disparities exist in PCa, with the incidence in African- Americans (AAs) being 50% higher than European Americans (EAs) and PCa mortality rates in AAs being more than two-fold higher. However, the disparity cannot be explained by screening, access to treatment, and genetics can only partially explain the disparity that does little to confer actionable clinical relevance. Currently, only 3 definitive risk factors for PCa have been identified: age, race, and family history of PCa. Smoking has not been an established risk factor for prostate cancer (PCa), and has not been emphasized in PCa prevention. However, recent studies have shown increasing evidence that there is a higher risk of biochemical recurrence, PCa mortality, and metastasis among current smokers, presenting an urgent need in re- evaluating the association between smoking and aggressive PCa. This study aimed to determine whether smoking increase the likelihood of developing a more aggressive prostate cancer. Methods. The study used data from the North Carolina–Louisiana Prostate Cancer Project (PCaP), which is a population-based study of incident PCa conducted between years 2004-2009 in 2 southern states where significant racial disparities in PCa are observed. Because PCa is over diagnosed and most PCa is not clinically relevant, this study will include only subjects with high (Gleason score ≥ 8; PSA & gt; 20 ng/mL; Gleason score = 7 and stage T3–T4) or low (Gleason score & lt; 7 and stage T1–T2 and PSA & lt;10 ng/mL) PCa aggressiveness. 1,497 participants were included in the analysis. Chi square and t-tests were used for the variables of interest and possible confounders, and multivariable logistic regression models were used for the odds ratio estimate. Results. There were 44.9% AAs and 55.1% EAs in the study. AA participants were significantly younger (mean=61.8, SD=7.9) compared with EAs (mean=64.0, SD=7.9), with lower education levels, shorter smoking cessation period, less screening tests in the past, less cigarettes per day, and higher Gleason sum. From the analysis, more AAs (57.6%) and those who were current smokers (22.7%) were diagnosed with high aggressive PCa. Current smokers had a 2.4 times- higher risk of high aggressive PCa (unadjusted OR=2.42, adjusted OR=2.39); when stratified by race, the risk diminished for EAs (OR=1.30) but increased for AAs (OR=3.36). Conclusion. Our study shows increased risk of aggressive PCa for current smokers, especially among AAs. Previous study had shown that self-reported cigarettes per day predicts smoke intake more poorly in AAs than in EAs. Thus, there is an urgent need in validated research using biomarkers to confirm the relationship of smoking and aggressive PCa, since cigarette smoking is preventable but have not been emphasized in PCa prevention. Citation Format: Ping-Ching Hsu, Shelbie Stahr, Christopher Brazeal, Elizabeth H. Fontham, L. Joseph Su. Smoking as a risk factor for the aggressive prostate cancer for African-American men from the North Carolina–Louisiana Prostate Cancer Project (PCaP) [abstract]. In: Proceedings of the AACR Virtual Conference: Thirteenth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2020 Oct 2-4. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2020;29(12 Suppl):Abstract nr PO-201.
    Type of Medium: Online Resource
    ISSN: 1055-9965 , 1538-7755
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2020
    detail.hit.zdb_id: 2036781-8
    detail.hit.zdb_id: 1153420-5
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