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Article ; Online: Telomere length: A possible link between phthalate exposure and cancer development?

Cai, Qiuyin

2016 Volume 6, Page(s) 6–7

MeSH term(s)	Humans ; Neoplasms ; Telomere ; Telomere Shortening
Language	English
Publishing date	2016-03-11
Publishing country	Netherlands
Document type	Journal Article ; Comment
ZDB-ID	2851331-9
ISSN	2352-3964
ISSN (online)	2352-3964
DOI	10.1016/j.ebiom.2016.03.016
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Zs.A 7090: Show issues

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Article ; Online: Genetic correlation and causal associations between psychiatric disorders and lung cancer risk.

Shi, Jiajun / Wen, Wanqing / Long, Jirong / Gamazon, Eric R / Tao, Ran / Cai, Qiuyin

Journal of affective disorders

2024 Volume 356, Page(s) 647–656

Abstract: Background: Patients with certain psychiatric disorders have increased lung cancer incidence. However, establishing a causal relationship through traditional epidemiological methods poses challenges.: Methods: Available summary statistics of genome- ... ...

Abstract	Background: Patients with certain psychiatric disorders have increased lung cancer incidence. However, establishing a causal relationship through traditional epidemiological methods poses challenges. Methods: Available summary statistics of genome-wide association studies of cigarette smoking, lung cancer, and eight psychiatric disorders, including attention deficit/hyperactivity disorder (ADHD), autism, depression, major depressive disorder, bipolar disorder, insomnia, neuroticism, and schizophrenia (range N: 46,350-1,331,010) were leveraged to estimate genetic correlations using Linkage Disequilibrium Score Regression and assess causal effect of each psychiatric disorder on lung cancer using two-sample Mendelian randomization (MR) models, comprising inverse-variance weighted (IVW), weighted median, MR-Egger, pleiotropy residual sum and outlier testing (MR-PRESSO), and a constrained maximum likelihood approach (cML-MR). Results: Significant positive correlations were observed between each psychiatric disorder and both smoking and lung cancer (all FDR < 0.05), except for the correlation between autism and lung cancer. Both univariable and the cML-MA MR analyses demonstrated that liability to schizophrenia, depression, ADHD, or insomnia was associated with an increased risk of overall lung cancer. Genetic liability to insomnia was linked specifically to squamous cell carcinoma (SCC), while genetic liability to ADHD was associated with an elevated risk of both SCC and small cell lung cancer (all P < 0.05). The later was further supported by multivariable MR analyses, which accounted for smoking. Limitations: Participants were constrained to European ancestry populations. Causal estimates from binary psychiatric disorders may be biased. Conclusion: Our findings suggest appropriate management of several psychiatric disorders, particularly ADHD, may potentially reduce the risk of developing lung cancer.
Language	English
Publishing date	2024-04-23
Publishing country	Netherlands
Document type	Journal Article
ZDB-ID	135449-8
ISSN	1573-2517 ; 0165-0327
ISSN (online)	1573-2517
ISSN	0165-0327
DOI	10.1016/j.jad.2024.04.080
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Zs.A 1485: Show issues

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Article ; Online: Associations between Folate and Alcohol Consumption with Colorectal Tumor Ki67 Expression in the Southern Community Cohort Study

Lawler, Thomas / Su, Timothy / Cai, Qiuyin / Steinwandel, Mark D. / Zheng, Wei / Warren Andersen, Shaneda

Nutrition and Cancer. 2023 Apr. 21, v. 75, no. 4 p.1211-1222

2023

Abstract: Folate is hypothesized to accelerate cell proliferation in colorectal cancer (CRC) by supporting DNA synthesis, while alcohol is also linked to gastrointestinal epithelial proliferation, despite biological antagonism of folate. We report associations ... ...

Abstract	Folate is hypothesized to accelerate cell proliferation in colorectal cancer (CRC) by supporting DNA synthesis, while alcohol is also linked to gastrointestinal epithelial proliferation, despite biological antagonism of folate. We report associations between folate and alcohol consumption with the proliferation marker Ki67 in CRC tumors from the Southern Community Cohort Study. Tumor samples were obtained from formalin-fixed paraffin-embedded tissue blocks. The percentage of cells expressing Ki67 was measured immunohistochemically. Exposures were assessed via questionnaire pre-diagnosis. Associations were assessed via linear regression. In 248 cases (40–78 years), neither dietary folate, folic acid supplements, nor total folate intake were associated with Ki67. Folic acid supplement use was associated with Ki67 in distal/rectal tumors (β [95% confidence interval]: 7.5 [1.2-13.8], p = .02) but not proximal tumors (-1.4 [-7.1-4.3], p=.62). A positive trend for total folate was observed for distal/rectal tumors (1.6 [0.0-3.3] per 200 μcg, p-trend=.05). Heavy drinking (women: ≥1 drink/day, men: ≥2 drinks/day) was associated with higher Ki67 (6.4 [1.0-11.9], vs. nondrinkers, p=.02), especially for distal/rectal tumors (10.4 [1.6-19.1], p=.02). Negative interaction between alcohol, total folate was observed for distal/rectal tumors (p-interaction=.06). Modest associations between folate, alcohol consumption and distal/rectal tumor Ki67 expression suggest accelerated proliferation, consistent with folate’s role in DNA synthesis.
Keywords	DNA replication ; alcohol drinking ; alcohols ; antagonism ; cell proliferation ; cohort studies ; colorectal neoplasms ; confidence interval ; epithelium ; folic acid ; gastrointestinal system ; immunohistochemistry ; nutrition ; questionnaires ; regression analysis
Language	English
Dates of publication	2023-0421
Size	p. 1211-1222.
Publishing place	Taylor & Francis
Document type	Article ; Online
ZDB-ID	424433-3
ISSN	1532-7914 ; 0163-5581
ISSN (online)	1532-7914
ISSN	0163-5581
DOI	10.1080/01635581.2023.2186264
Database	NAL-Catalogue (AGRICOLA)

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Zs.A 1496: Show issues

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Article ; Online: Genetic correlation and causal associations between circulating C-reactive protein levels and lung cancer risk.

Shi, Jiajun / Wen, Wanqing / Long, Jirong / Xue, Haoran / Yang, Yaohua / Tao, Ran / Pan, Wei / Shu, Xiao-Ou / Cai, Qiuyin

Cancer causes & control : CCC

2024

Abstract: Purpose: We aimed to characterize genetic correlations and causal associations between circulating C-reactive protein (CRP) levels and the risk of lung cancer (LC).: Methods: Leveraging summary statistics from genome-wide association studies of ... ...

Abstract	Purpose: We aimed to characterize genetic correlations and causal associations between circulating C-reactive protein (CRP) levels and the risk of lung cancer (LC). Methods: Leveraging summary statistics from genome-wide association studies of circulating CRP levels among 575,531 individuals of European ancestry, and LC risk among 29,266 cases and 56,450 controls, we investigated genetic associations of circulating CRP levels with the risk of overall lung cancer and its histological subtypes, by using linkage disequilibrium score (LDSC) regression and Mendelian randomization (MR) analyses. Results: Significant positive genetic correlations between circulating CRP levels and the risk of LC and its histological subtypes were identified from LDSC regression, with correlation coefficients ranging from 0.12 to 0.26, and all false discovery adjusted p < 0.05. Univariable MR demonstrated a nominal association between CRP levels and an increased risk of lung squamous cell carcinoma (SCC) (inverse variance-weighted OR = 1.15, 95% CI 1.01-1.30). However, this association disappeared when multivariable MR included cigarettes per day and/or body mass index. By using our recently developed constrained maximum likelihood-based MR method, we identified significant associations of CRP levels with the risk of overall LC (OR 1.06, 95% CI 1.03-1.09), SCC (OR 1.06, 95% CI 1.02-1.09), and small cell lung cancer (SCLC, OR 1.09, 95% CI 1.03-1.15). Moreover, most univariable and multivariable MR analyses also revealed consistent CRP-SCLC associations. Conclusion: There may be a genetic and causal association between circulating CRP levels and the risk of SCLC, which is in line with previous population-based observational studies.
Language	English
Publishing date	2024-02-08
Publishing country	Netherlands
Document type	Journal Article
ZDB-ID	1064022-8
ISSN	1573-7225 ; 0957-5243
ISSN (online)	1573-7225
ISSN	0957-5243
DOI	10.1007/s10552-024-01855-7
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Zs.A 3375: Show issues

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Article ; Online: Diet quality and lung cancer incidence in a low-income population in the United States.

Munro, Heather M / Yu, Danxia / Zheng, Wei / Blot, William J / Cai, Qiuyin / Shrubsole, Martha J

British journal of cancer

2023 Volume 129, Issue 4, Page(s) 626–635

Abstract: Background: Although tobacco smoking is the leading cause of lung cancer, interest in the relationship of diet quality on risk has been growing.: Methods: We examined the association between Healthy Eating Index-2010 (HEI-10) at enrollment and lung ... ...

Abstract	Background: Although tobacco smoking is the leading cause of lung cancer, interest in the relationship of diet quality on risk has been growing. Methods: We examined the association between Healthy Eating Index-2010 (HEI-10) at enrollment and lung cancer incidence among 70,802 participants in a predominantly African American and low-income prospective cohort in the southern United States. Outcomes were ascertained through linkages with state cancer registries and the National Death Index (NDI). Hazard ratios by HEI-10 quartiles were assessed using Cox proportional hazard models adjusted for potential confounders. Results: During ≤16 years of follow-up, 1454 incident lung cancers were identified. The lowest HEI-10 quartile compared to the highest was adversely associated with lung cancer risk (HR: 1.89, 95% CI 1.16-3.07) among male former smokers and female never smokers (HR: 2.58, 95% CI 1.06-6.28). Conclusions: Low-quality diet was associated with increased lung cancer risk among male former smokers and female never smokers but cautious interpretation of the findings should be taken due to the small number of lung cancers among never smokers and the possibility of residual confounding by smoking in ever smokers.
MeSH term(s)	Humans ; Male ; United States/epidemiology ; Female ; Risk Factors ; Prospective Studies ; Incidence ; Diet/adverse effects ; Poverty ; Lung Neoplasms/epidemiology ; Lung Neoplasms/etiology ; Proportional Hazards Models
Language	English
Publishing date	2023-07-03
Publishing country	England
Document type	Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID	80075-2
ISSN	1532-1827 ; 0007-0920
ISSN (online)	1532-1827
ISSN	0007-0920
DOI	10.1038/s41416-023-02342-7
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Uh III Zs.142: Show issues

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Article ; Online: Associations between Folate and Alcohol Consumption with Colorectal Tumor Ki67 Expression in the Southern Community Cohort Study.

Lawler, Thomas / Su, Timothy / Cai, Qiuyin / Steinwandel, Mark D / Zheng, Wei / Warren Andersen, Shaneda

Nutrition and cancer

2023 Volume 75, Issue 4, Page(s) 1211–1222

Abstract	Folate is hypothesized to accelerate cell proliferation in colorectal cancer (CRC) by supporting DNA synthesis, while alcohol is also linked to gastrointestinal epithelial proliferation, despite biological antagonism of folate. We report associations between folate and alcohol consumption with the proliferation marker Ki67 in CRC tumors from the Southern Community Cohort Study. Tumor samples were obtained from formalin-fixed paraffin-embedded tissue blocks. The percentage of cells expressing Ki67 was measured immunohistochemically. Exposures were assessed via questionnaire pre-diagnosis. Associations were assessed via linear regression. In 248 cases (40-78 years), neither dietary folate, folic acid supplements, nor total folate intake were associated with Ki67. Folic acid supplement use was associated with Ki67 in distal/rectal tumors (β [95% confidence interval]: 7.5 [1.2-13.8],
MeSH term(s)	Male ; Humans ; Female ; Folic Acid ; Cohort Studies ; Ki-67 Antigen ; Colorectal Neoplasms/epidemiology ; Colorectal Neoplasms/genetics ; Alcohol Drinking/adverse effects ; Rectal Neoplasms ; DNA ; Risk Factors
Chemical Substances	Folic Acid (935E97BOY8) ; Ki-67 Antigen ; DNA (9007-49-2)
Language	English
Publishing date	2023-03-12
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID	424433-3
ISSN	1532-7914 ; 0163-5581
ISSN (online)	1532-7914
ISSN	0163-5581
DOI	10.1080/01635581.2023.2186264
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Zs.A 1496: Show issues

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Article ; Online: Association of Urinary N7-(1-hydroxyl-3-buten-1-yl) Guanine (EB-GII) Adducts and Butadiene-Mercapturic Acids with Lung Cancer Development in Cigarette Smokers.

Jokipii Krueger, Caitlin C / Park, Sungshim L / Patel, Yesha / Stram, Daniel O / Aldrich, Melinda / Cai, Qiuyin / Tretyakova, Natalia Y

Chemical research in toxicology

2024 Volume 37, Issue 2, Page(s) 374–384

Abstract: Approximately 10% of smokers will develop lung cancer. Sensitive predictive biomarkers are needed to identify susceptible individuals. 1,3-Butadiene (BD) is among the most abundant tobacco smoke carcinogens. BD is metabolically activated to 3,4-epoxy-1- ... ...

Abstract	Approximately 10% of smokers will develop lung cancer. Sensitive predictive biomarkers are needed to identify susceptible individuals. 1,3-Butadiene (BD) is among the most abundant tobacco smoke carcinogens. BD is metabolically activated to 3,4-epoxy-1-butene (EB), which is detoxified via the glutathione conjugation/mercapturic acid pathway to form monohydroxybutenyl mercapturic acid (MHBMA) and dihydroxybutyl mercapturic acid (DHBMA). Alternatively, EB can react with guanine nucleobases of DNA to form N7-(1-hydroxyl-3-buten-1-yl) guanine (EB-GII) adducts. We employed isotope dilution LC/ESI-HRMS/MS methodologies to quantify MHBMA, DHBMA, and EB-GII in urine of smokers who developed lung cancer (
MeSH term(s)	Humans ; Smokers ; Butadienes/metabolism ; Acetylcysteine/metabolism ; Lung Neoplasms/chemically induced ; Guanine ; Biomarkers/urine ; Tobacco Products ; DNA Adducts
Chemical Substances	1,3-butadiene (JSD5FGP5VD) ; Butadienes ; Acetylcysteine (WYQ7N0BPYC) ; Guanine (5Z93L87A1R) ; Biomarkers ; DNA Adducts
Language	English
Publishing date	2024-02-05
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID	639353-6
ISSN	1520-5010 ; 0893-228X
ISSN (online)	1520-5010
ISSN	0893-228X
DOI	10.1021/acs.chemrestox.3c00336
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Zs.A 2320: Show issues

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Article ; Online: Drug-target Mendelian randomization revealed a significant association of genetically proxied metformin effects with increased prostate cancer risk.

Sun, Xiaohui / Ping, Jie / Guo, Xingyi / Long, Jirong / Cai, Qiuyin / Shu, Xiao-Ou / Shu, Xiang

Molecular carcinogenesis

2024 Volume 63, Issue 5, Page(s) 849–858

Abstract: The association between metformin use and risk of prostate cancer remains controversial, while data from randomized trials is lacking. We aim to evaluate the association of genetically proxied metformin effects with prostate cancer risk using a drug- ... ...

Abstract	The association between metformin use and risk of prostate cancer remains controversial, while data from randomized trials is lacking. We aim to evaluate the association of genetically proxied metformin effects with prostate cancer risk using a drug-target Mendelian randomization (MR) approach. Summary statistics for prostate cancer were obtained from the Prostate Cancer Association Group to Investigate Cancer Associated Alterations in the Genome Consortium (79,148 cases and 61,106 controls). Cis-expression quantitative trait loci (cis-eQTL) variants in the gene targets of metformin were identified in the GTEx project and eQTLGen consortium. We also obtained male-specific genome-wide association study data for type 2 diabetes, body mass index (BMI), total testosterone, bioavailable testosterone, estradiol, and sex hormone binding globulin for mediation analysis. Inverse-variance weighted (IVW) regression, weighted median, MR-Egger regression, and MR-PRESSO were performed in the main MR analysis. Multivariable MR was used to identify potential mediators and genetic colocalization analysis was performed to assess any shared genetic basis between two traits of interest. We found that genetically proxied metformin effects (1-SD HbA
MeSH term(s)	Male ; Humans ; Metformin/therapeutic use ; Diabetes Mellitus, Type 2/drug therapy ; Diabetes Mellitus, Type 2/genetics ; Genome-Wide Association Study ; Mendelian Randomization Analysis ; Prostatic Neoplasms/drug therapy ; Prostatic Neoplasms/genetics ; Testosterone ; Polymorphism, Single Nucleotide
Chemical Substances	Metformin (9100L32L2N) ; Testosterone (3XMK78S47O)
Language	English
Publishing date	2024-03-22
Publishing country	United States
Document type	Journal Article
ZDB-ID	1004029-8
ISSN	1098-2744 ; 0899-1987
ISSN (online)	1098-2744
ISSN	0899-1987
DOI	10.1002/mc.23692
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Zs.A 2664: Show issues

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Article ; Online: Association of urinary prostaglandin E2 metabolite and mortality among adults.

Wen, Wanqing / Yang, Gong / Cai, Qiuyin / Shu, Xiao-Ou / Zheng, Wei

Scientific reports

2022 Volume 12, Issue 1, Page(s) 18905

Abstract: Prostaglandins play a critical role in inflammatory response. To investigate the association of urinary PGE-M, a stable end-product of prostaglandin E2 ( ... ...

Abstract	Prostaglandins play a critical role in inflammatory response. To investigate the association of urinary PGE-M, a stable end-product of prostaglandin E2 (PGE
MeSH term(s)	Adult ; Male ; Humans ; Female ; Dinoprostone ; China/epidemiology ; Case-Control Studies ; Cohort Studies ; Prostaglandins E ; Cardiovascular Diseases ; Risk Factors
Chemical Substances	Dinoprostone (K7Q1JQR04M) ; Prostaglandins E
Language	English
Publishing date	2022-11-07
Publishing country	England
Document type	Journal Article
ZDB-ID	2615211-3
ISSN	2045-2322 ; 2045-2322
ISSN (online)	2045-2322
ISSN	2045-2322
DOI	10.1038/s41598-022-23773-x
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Article ; Online: The putative oncogenic role of WDTC1 in colorectal cancer.

Wang, Xiaoyu / Cai, Qiuyin / Ping, Jie / Diaz-Zabala, Hector / Xia, Yumin / Guo, Xingyi

Carcinogenesis

2022 Volume 43, Issue 6, Page(s) 594–600

Abstract: Microsatellite instability (MSI) is detected in approximately 15% of colorectal cancers (CRCs). WD40 and tetratricopeptide repeats 1 (WDTC1) is frequently mutated in MSI CRC, indicating that it may contribute to CRC development. However, the functional ... ...

Abstract	Microsatellite instability (MSI) is detected in approximately 15% of colorectal cancers (CRCs). WD40 and tetratricopeptide repeats 1 (WDTC1) is frequently mutated in MSI CRC, indicating that it may contribute to CRC development. However, the functional evidence of the role of WDTC1 in CRC development remains unknown. Herein, we conducted in vitro assays to examine the function of WDTC1 using knockdown experiments in three CRC cell lines, SW480, CACO2, and LoVo. We provided strong evidence that silencing WDTC1 significantly suppressed cell proliferation, migration, and invasion consistently in all three CRC cell lines. To evaluate the potential role of WDTC1 in regulating CRC-related genes, we conducted RNA sequencing after 24 and 48 h in SW480 cells after treating WDTC1-siRNA and its vehicle control cells. Differential gene expression analysis identified 44 (42 downregulated and 2 upregulated) and 16 (all downregulated) genes, at time points of 24 and 48 h, respectively, whereas 15 downregulated genes were commonly detected at both time points. The ingenuity pathways analysis suggested that the most significant enrichments associated with cancer function and upstream regulator ATM/ATR were observed for these commonly observed genes. We further verified differential gene expression of eight cancer-related genes, ARHGEF12, GSTP1, FNDC3A, TMTC3, RTN4, RRM2, UHMK1, and PTPRF, using RT-PCR in all three cell lines. Our findings provided additional insight into the oncogenic role of WDTC1 in CRC development.
MeSH term(s)	Humans ; Caco-2 Cells ; Carcinogenesis/genetics ; Carrier Proteins/genetics ; Colorectal Neoplasms/genetics ; Colorectal Neoplasms/metabolism ; Fibronectins/genetics ; Membrane Proteins/genetics ; Microsatellite Instability ; Oncogenes/genetics
Chemical Substances	Carrier Proteins ; Fibronectins ; FNDC3A protein, human ; Membrane Proteins ; TMTC3 protein, human ; WDTC1 protein, human
Language	English
Publishing date	2022-03-03
Publishing country	England
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID	603134-1
ISSN	1460-2180 ; 0143-3334
ISSN (online)	1460-2180
ISSN	0143-3334
DOI	10.1093/carcin/bgac027
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