Five common haplotype-tagging variants of adiponectin (ADIPOQ) and cancer susceptibility: a meta-analysis.

Abstract:

AIMS:The relationship between common haplotype-tagging polymorphisms (rs266729 [11365C>G], rs822395 [-4034A>C], rs822396 [-3964A>G], rs2241766 [45T>G], and rs1501299 [276G>T]) in the ADIPOQ gene and cancer risk has been investigated in different ethnic groups; however, these studies have yielded contradictory results. With this in mind, this meta-analysis was performed in an attempt to draw a more precise conclusion regarding the association between ADIPOQ polymorphisms and cancer risk. RESULTS:In this study, with a total of 19 eligible articles consisting of 52 studies, the pooled odds ratios (ORs) for the association between ADIPOQ rs1501299 and cancer risk were statistically significant (dominant model, TT/GT vs. GG, OR=0.84, 95% confidence interval [CI]: 0.77-0.92; homozygous model, TT vs. GG, OR=0.80, 95% CI: 0.68-0.94). These results suggested that ADIPOQ rs1501299 might be a protection-associated polymorphism in cancer. The stratified analyses indicated that the variant T allele of ADIPOQ rs1501299 was associated with decreased risk of cancer in both Caucasian and Asian populations when compared with the G allele. No significant association for the rest of the polymorphisms was observed under any genetic model. CONCLUSIONS:This meta-analysis suggests that the ADIPOQ rs1501299 may be a protective factor for carcinogenesis.

authors

Li Q,Ma Y,Sang W,Cui W,Li X,Liu X,Zhang W

doi

10.1089/gtmb.2013.0493

subject

Has Abstract

pub_date

2014-06-01 00:00:00

pages

417-24

issue

6

eissn

1945-0265

issn

1945-0257

journal_volume

18

pub_type

杂志文章,meta分析
  • Associations between single-nucleotide polymorphisms and epidural ropivacaine consumption in patients undergoing breast cancer surgery.

    abstract::Up to date, few published studies indicated the associations between genetic polymorphisms and epidural local anesthetics consumption. In this study, we investigated the associations between seven single-nucleotide polymorphisms (SNPs) and epidural ropivacaine consumption during breast cancer surgery in women from nor...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2012.0388

    authors: Liu J,Jiang Y,Pang D,Xi H,Liu Y,Li W

    更新日期:2013-06-01 00:00:00

  • Genetic Polymorphisms of Cytochrome P450 Enzymes and Transport Proteins in a Russian Population and Three Ethnic Groups of Dagestan.

    abstract:AIM:The objective of this study was to investigate the prevalence of polymorphic markers of the CYP2C19, CYP2C9, CYP2D6, SLCO1B1, and ABCB1 genes among the three ethnic groups in Dagestan and compare it with the carrier frequency of these markers among the Russian population living in Moscow. METHODS:The study involve...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2017.0036

    authors: Mirzaev KB,Sychev DA,Ryzhikova KA,Konova OD,Mammaev SN,Gafurov DM,Shuev GN,Grishina EA,Sozaeva ZA

    更新日期:2017-12-01 00:00:00

  • Methylation of the Sclerostin (SOST) Gene in Serum Free DNA: A New Bone Biomarker?

    abstract:: Introduction: Cell-free DNA (cfDNA) methylation is an important molecular biomarker, which provides information about the regulation of gene expression in the tissue of origin. There is an inverse correlation between SOST gene methylation and expression levels. ...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2020.0172

    authors: Del Real A,Perez-Campo FM,Perez-Nuñez MI,Sañudo C,Santurtun A,Garcia-Ibarbia C,Garcia-Unzueta MT,Fraga MF,Fernandez AF,Valero MC,Laguna E,Riancho JA

    更新日期:2021-01-01 00:00:00

  • Design of a Targeted Sequencing Assay to Detect Rare Mutations in Circulating Tumor DNA.

    abstract:BACKGROUND:Qualitative and quantitative detection of circulating tumor DNA (ctDNA) is a liquid biopsy technology used for early cancer diagnosis. However, the plasma ctDNA content is extremely low, so it is difficult to detect somatic mutations of tumors using conventional sequencing methods. Target region sequencing (...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2018.0173

    authors: Chen J,Chen J,He F,Huang Y,Lu S,Fan H,Wang M,Xu R

    更新日期:2019-04-01 00:00:00

  • Association of androgen receptor, prostate-specific antigen, and CYP19 gene polymorphisms with prostate carcinoma and benign prostatic hyperplasia in a north Indian population.

    abstract::The genes involved in androgen pathway and metabolism have been reported to contribute considerably to prostate carcinoma (CaP) risk. The present study investigated the association of androgen receptor (AR), prostate-specific antigen (PSA or KLK3), and cytochrome P450 (CYP19) gene polymorphisms in CaP (n=105) and beni...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2011.0322

    authors: Soni A,Bansal A,Mishra AK,Batra J,Singh LC,Chakraborty A,Yadav DS,Mohanty NK,Saxena S

    更新日期:2012-08-01 00:00:00

  • Analysis of CLCN2 as candidate gene for megalencephalic leukoencephalopathy with subcortical cysts.

    abstract::Mutations in the gene MLC1 are found in approximately 80% of the patients with the inherited childhood white matter disorder megalencephalic leukoencephalopathy with subcortical cysts (MLC). Genetic linkage studies have not led to the identification of another disease gene. We questioned whether mutations in CLCN2, co...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2009.0148

    authors: Scheper GC,van Berkel CG,Leisle L,de Groot KE,Errami A,Jentsch TJ,Van der Knaap MS

    更新日期:2010-04-01 00:00:00

  • High-resolution melting analysis of MED12 mutations in uterine leiomyomas in Chinese patients.

    abstract:OBJECTIVES:Somatic mutations in mediator complex subunit 12 (MED12) have emerged as a critical genetic change in the development of uterine leiomyomas. Studies, however, have focused largely on cohorts consisting of Caucasian patients. In this study, uterine leiomyomas from Chinese patients were examined for MED12 muta...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2014.0273

    authors: Wang H,Ye J,Qian H,Zhou R,Jiang J,Ye L

    更新日期:2015-03-01 00:00:00

  • DEFB4A Promoter Polymorphism Is Associated with Chronic Periodontitis: A Case-Control Study.

    abstract:: Background: Human β-defensin-2 is an antimicrobial peptide with antibiotic properties secreted by the oral cavity to protect the host against microbial attack. The inter-individual differences in defensin expression profiles due to genetic variation might be partly respons...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2019.0218

    authors: Kurt-Bayrakdar S,Ozturk A,Kara N

    更新日期:2020-03-01 00:00:00

  • Distribution of the IL-1RN, IL-6, IL-10, INF-γ, and TNF-α Gene Polymorphisms in the Mexican Population.

    abstract:BACKGROUND:Cytokines are a group of polypeptides with an important role in the inflammatory response. It has been suggested that certain polymorphisms located in several cytokine genes are associated with different diseases. The aim of the present study was to establish the gene frequency of 13 polymorphisms of the IL-...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2012.0100

    authors: Vargas-Alarcon G,Ramírez-Bello J,Juárez-Cedillo T,Ramírez-Fuentes S,Carrillo-Sánchez S,Fragoso JM

    更新日期:2012-10-01 00:00:00

  • Genetic Polymorphisms in PRM1, PRM2, and YBX2 Genes are Associated with Male Factor Infertility.

    abstract:AIMS:The etiology of infertility is still unknown in almost half of all male infertility patients. In sperm, DNA condensation differs from somatic and female gamete cells, with the protamine (PRM) gene and its transcription factor, Y-box binding protein 2 (YBX2), playing key roles in making the structure more compact. ...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2017.0040

    authors: Aydos OSE,Hekmatshoar Y,Altınok B,Özkan T,Şakirağaoğlu O,Karadağ A,Kaplan F,Ilgaz S,Taşpınar M,Yükselen I,Sunguroğlu A,Aydos K

    更新日期:2018-01-01 00:00:00

  • A real-time polymerase chain reaction-based protocol for low/medium-throughput Y-chromosome microdeletions analysis.

    abstract:PURPOSE:We describe a real-time polymerase chain reaction (PCR) protocol based on the fluorescent molecule SYBR Green chemistry, for a low- to medium-throughput analysis of Y-chromosome microdeletions, optimized according to the European guidelines and aimed at making the protocol faster, avoiding post-PCR processing, ...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2012.0220

    authors: Segat L,Padovan L,Doc D,Petix V,Morgutti M,Crovella S,Ricci G

    更新日期:2012-12-01 00:00:00

  • Dystrophin gene mutation analysis in Iranian males and females using multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification methods.

    abstract::Duchenne's muscular dystrophy and Becker muscular dystrophy (BMD) are X-linked recessive disorders caused by mutations in the dystrophin gene. In this project, 100 unrelated male patients were initially screened for deletions in the dystrophin gene by multiplex polymerase chain reaction, of whom 52 were positive. We p...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2011.0057

    authors: Khordadpoor-Deilamani F,Akbari MT,Nafissi S,Zamani G

    更新日期:2011-12-01 00:00:00

  • Assessment of individual susceptibility to baseline DNA and cytogenetic damage in a healthy Turkish population: evaluation with lifestyle factors.

    abstract:BACKGROUND:Cytogenetic biomarkers are most frequently used well-established endpoints in human population studies with their sensitivity for measuring exposure to genotoxic agents. They have an important role as early predictors of cancer risk. Identification of individual genotypes of metabolic gene polymorphisms help...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2012.0038

    authors: Kadioglu E,Kocabas NA,Demircigil GC,Coskun E,Ozcagli E,Durmaz E,Karahalil B,Burgaz S,Sardas S

    更新日期:2012-10-01 00:00:00

  • Association of angiotensin converting enzyme (insertion/deletion) gene polymorphism with essential hypertension in northern Indian subjects.

    abstract:OBJECTIVE:Essential hypertension is a multifactorial disease in which genetic and environmental factors play an important role. The renin-angiotensin system (RAS) is known to play a critical role in the homeostasis of blood pressure. Angiotensin-I converting enzyme (ACE) is a significant component of RAS, and an insert...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2011.0155

    authors: Srivastava K,Sundriyal R,Meena PC,Bhatia J,Narang R,Saluja D

    更新日期:2012-03-01 00:00:00

  • A one-step prescreening for point mutations and large rearrangement in BRCA1 and BRCA2 genes using quantitative polymerase chain reaction and high-resolution melting curve analysis.

    abstract::High-resolution melting (HRM) of DNA is a versatile method for mutation scanning that monitors the fluorescence of double-strand DNA with saturating dye. Performing HRM on a real-time thermocycler enables semiquantitative analysis (quantitative polymerase chain reaction, qPCR) to be associated to HRM analysis for dete...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2009.0183

    authors: Coulet F,Pires F,Rouleau E,Lefol C,Martin S,Colas C,Cohen-Haguenauer O,Giurgea I,Fajac A,Noguès C,Demange L,Hardouin A,Lidereau R,Soubrier F

    更新日期:2010-10-01 00:00:00

  • A c.1363C>T (p.R455X) nonsense mutation of RB1 gene in a southern Chinese retinoblastoma pedigree.

    abstract::Retinoblastoma (RB) is the most common malignant intraocular tumor in children. Fifty percent of RB patients are carriers of a predisposing germline mutation with high penetrance. RB1 has been identified as the only pathological gene. We present the rapid detection of an RB1 gene mutation in a Han pedigree of two RB p...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2009.0162

    authors: Chen CY,Xu CM,Du ZF,Chen XL,Ren GL,Zhang XN

    更新日期:2010-04-01 00:00:00

  • Toll-like receptor 6 and connective tissue growth factor are significantly upregulated in mitomycin-C-treated urothelial carcinoma cells under hydrostatic pressure stimulation.

    abstract:BACKGROUND:Urothelial carcinoma (UC) is the most common histologic subtype of bladder cancer. The administration of mitomycin C (MMC) into the bladder after transurethral resection of the bladder tumor (TURBT) is a common treatment strategy for preventing recurrence after surgery. We previously applied hydrostatic pres...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2013.0443

    authors: Chen SK,Chung CA,Cheng YC,Huang CJ,Chen WY,Ruaan RC,Li C,Tsao CW,Hu WW,Chien CC

    更新日期:2014-06-01 00:00:00

  • Genetic epidemiology of cancer predisposition DNA repair genes is probably related with ancestral surviving under adverse environmental conditions.

    abstract:AIMS:Surviving under a stressful environment may be a real challenge. Individuals (and their offspring) with accumulated genetic variation in their DNA repair genes may have a higher probability to survive under these conditions. A partially unstable DNA repair system raises the mutagenesis rate and the probability for...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2014.0053

    authors: Voskarides K

    更新日期:2014-08-01 00:00:00

  • Genetic polymorphisms of platelet receptors in patients with acute myocardial infarction and resistance to antiplatelet therapy.

    abstract:METHODS:The studied group comprises 124 patients with acute myocardial infarction on dual antiplatelet therapy with acetylsalicylic acid (ASA) and thienopyridines. Antiplatelet therapy was monitored by platelet-rich plasma light transmittance aggregometry (LTA) using the APACT 4004 analyzer (Helena Laboratories) and by...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2014.0077

    authors: Ulehlova J,Slavik L,Kucerova J,Krcova V,Vaclavik J,Indrak K

    更新日期:2014-09-01 00:00:00

  • A novel splice site and two known mutations of androgen receptor gene in sex-reversed XY phenotype.

    abstract::Molecular characterization of 27 cytogenetically confirmed Indian XY females was attempted by screening selected regions of candidate genes namely SRY (HMG box) and the ligand-binding domain of androgen receptor (AR) (Exons 5-8). Three of the index cases showed sequence variations in exons of the AR gene: a deletion m...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 临床试验,杂志文章,评审

    doi:10.1089/gtmb.2011.0292

    authors: Vasu VR,Saranya B,Jayashankar M,Munirajan AK,Santhiya ST

    更新日期:2012-07-01 00:00:00

  • Screening for AZFc partial deletions in Dravidian men with nonobstructive azoospermia and oligozoospermia.

    abstract:CONTEXT:Dravidians are the predominant population residing in South India with a diverse genetic structure. Considering various genetic discoveries taking place today, it is evident that deletions in the AZFc region are the most common cause of severe spermatogenic failure (SSF) in various populations studied. However,...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2014.0251

    authors: Vijesh VV,Nambiar V,Mohammed SI,Sukumaran S,Suganthi R

    更新日期:2015-03-01 00:00:00

  • Identification of Potential Hub Genes and Signal Pathways Promoting the Distinct Biological Features of Cord Blood-Derived Endothelial Progenitor Cells Via Bioinformatics.

    abstract:: Background: Numerous studies, ranging from the alleviation of tissue ischemia to the assessment of cancer prognosis, have demonstrated the fundamental biological differences between human umbilical cord blood-derived endothelial progenitor cells (CB-EPCs) and adult periphe...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2019.0272

    authors: Wang Q,Chen S,Wu J,Liu D,Jiang N,Wang B,Zhai J,Liu Z

    更新日期:2020-09-01 00:00:00

  • Genotyping the GGGCGG tandem repeat promoter polymorphism in the 5-lipoxygenase enzyme gene (ALOX5) by pyrosequencing assay.

    abstract:AIMS:Efficient genotyping methods for many biologically significant repeat genetic polymorphisms, particularly in GC-rich regions of the genome, are limited. In particular, a short tandem repeat polymorphism [GGCGGG] in the promoter region of ALOX5 has been implicated as an important marker for inflammatory diseases. W...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2008.0103

    authors: Schentrup AM,Allayee H,Lima JJ,Johnson JA,Langaee TY

    更新日期:2009-06-01 00:00:00

  • Genetic Polymorphism of the Serotonin Transporter Gene, SLC6A4 rs16965628, Is Associated with Obsessive Compulsive Disorder.

    abstract::Obsessive compulsive disorder (OCD) is a psychiatric disorder characterized by obsessive ideas and compulsive behaviors. Genetic studies have centered on candidate genes involved in OCD etiology related to serotonergic and dopaminergic systems. In this study, the relationship between cathechol-O-methyltransferase (COM...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2014.0319

    authors: Cengiz M,Okutan SN,Bayoglu B,Sakalli Kani A,Bayar R,Kocabasoglu N

    更新日期:2015-05-01 00:00:00

  • Gene Polymorphisms in the RANKL/RANK/OPG Pathway Are Associated with Type 2 Diabetes Mellitus in Southern Han Chinese Women.

    abstract:AIMS:Receptor activator of nuclear factor-kappa B ligand (RANKL), its receptor activator of nuclear factor-kappa B (RANK), and decoy receptor osteoprotegerin (OPG) are three major proteins of the RANKL/RANK/OPG signaling pathway encoded by TNFSF11, TNFRSF11A, and TNFRSF11B, respectively. This pathway plays a critical r...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2015.0306

    authors: Duan P,Tu P,Si L,Hu W,Liu M,Liu J,Xue Y

    更新日期:2016-06-01 00:00:00

  • Polymorphism of ERCC2 Asp312Asn with lung cancer risk: evidence from 20,101 subjects.

    abstract::The association between excision repair cross complementing group 2 (ERCC2) Asp312Asn polymorphism and lung cancer has been reported by many articles recently, but the results were controversial and inconclusive. Therefore, a meta-analysis was conducted to assess the relationship between them. Pooled odds ratios (ORs)...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章,meta分析

    doi:10.1089/gtmb.2013.0296

    authors: Tan X,Wang Y,Shi L,Xian L,Guo J,Liang G,Chen M

    更新日期:2014-01-01 00:00:00

  • PARP-1 rs3219073 polymorphism may contribute to susceptibility to lung cancer.

    abstract:OBJECTIVE:To investigate the relationship between the PARP-1 rs3219073 C>G polymorphism and susceptibility to lung cancer in Chinese people. METHODS:In accordance with the case-control study principle, 645 of the patients had histologically recognized primary lung cancer, among them 240 had squamous carcinoma, 217 had...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 临床试验,杂志文章

    doi:10.1089/gtmb.2014.0106

    authors: Wang HT,Gao Y,Zhao YX,Yu H,Wang TL,Bai L,Chen YZ,Zhang HB,Zhou BS,Qu YL,Liu D,Chen Y

    更新日期:2014-11-01 00:00:00

  • A Meta-analysis on the Effect of Ulinastatin on Serum Levels of C-Reactive Protein, Interleukin 6, and Tumor Necrosis Factor Alpha in Asian Patients with Acute Pancreatitis.

    abstract:OBJECTIVES:We aimed to investigate the influence of ulinastatin (UTI) on the serum levels of C-reactive protein (CRP), interleukin 6 (IL-6), and tumor necrosis factor alpha (TNF-α) in Asian patients with acute pancreatitis (AP) by performance of a meta-analysis. METHODS:Two investigators independently searched 11 data...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章,meta分析

    doi:10.1089/gtmb.2015.0192

    authors: Zhang C,Wang Y,Fu W,Zhang W,Wang T,Qin H

    更新日期:2016-03-01 00:00:00

  • A Comparative Study of ARHI Imprinted Gene Detection and Fine-Needle Aspiration Cytology in the Differential Diagnosis of Benign and Malignant Thyroid Nodules.

    abstract:: Aims: To compare fine-needle aspiration cytology (FNAC) with imprinted gene detection in the differential diagnosis of benign and malignant thyroid nodules. Methods: A total of 34 patients (35 cases of thyroid nodules) were exa...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 杂志文章

    doi:10.1089/gtmb.2019.0028

    authors: Zou D,Wu C,Miao J,Shao Q,Huang W,Huang J,Wu G,Zhang Q

    更新日期:2019-09-01 00:00:00

  • Association of -2518A>G promoter polymorphism in the monocyte chemoattractant protein-1 (MCP-1) gene with type 2 diabetes and coronary artery disease.

    abstract:AIMS:Inflammatory markers play an important role in the development of diseases related to metabolic syndrome, such as type 2 diabetes (T2D) and coronary artery disease (CAD). The present study evaluates the association of -2518A>G polymorphism in the monocyte chemoattractant protein-1 (MCP-1) gene with T2D and CAD. R...

    journal_title:Genetic testing and molecular biomarkers

    pub_type: 临床试验,杂志文章

    doi:10.1089/gtmb.2013.0227

    authors: Kaur R,Matharoo K,Arora P,Bhanwer AJ

    更新日期:2013-10-01 00:00:00