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  1. Article ; Online: First Report of Colletotrichum siamense Causing Leaf Spot on Jasminum sambac in China

    Sun, Mingyan / Li, Chunniu / Li, Xianmin / Bu, Zhaoyang / La, Yanfei / Liu, Kedan / Li, Qili

    Plant Disease. 2023 July 01, v. 107, no. 7 p.2225-

    2023  

    Abstract: Jasmine (Jasminum sambac (L.) Aiton) is cultivated as a commercial floricultural crop in many countries around the world (Gao et al. 2020). From June to August 2020, leaf spots on jasmine were observed on a jasmine plantation in Hengzhou, Guangxi ... ...

    Abstract Jasmine (Jasminum sambac (L.) Aiton) is cultivated as a commercial floricultural crop in many countries around the world (Gao et al. 2020). From June to August 2020, leaf spots on jasmine were observed on a jasmine plantation in Hengzhou, Guangxi province. Over 40% of the plants in 6 ha fields were infected. This disease was prevalent in jasmine production areas of China (Chen et al. 2012; Du et al. 2020). Symptoms began as chlorotic regions (from 5 to 10 mm in diameter) with light brown necrotic centers, which gradually expanded to the entire leaf. Eventually, the disease led to defoliation and dieback. The edges of affected parts from diseased leaves were cut into pieces (3 mm²). Pieces were treated with 75% ethanol for 10 s, soaked in 2% NaClO solution for 1 min, washed three times with sterile water, and incubated on potato dextrose agar (PDA) plates at 28°C for 5 days in the dark. Fungal cultures that showed similar morphological characteristics were isolated, and three representative isolates (HL6-1 to HL6-3) were purified following Mo et al. (2018). The cultures on PDA changed from white to dark gray after 7 days and produced conidiomata after 14 days. Conidia were hyaline, one celled, guttulate, cylindrical, and 12.07 to 18.09 × 4.04 to 8.05 μm, 13.17 to 16.35 × 4.22 to 6.13 μm, and 10.11 to 22.17 × 3.65 to 8.1 μm for HL6-1, HL6-2, and HL6-3, respectively. Gray-brown or dark brown appressoria formed from conidia were subglobose or elliptical. Conidial appressoria and mycelial appressoria were 5.53 to 13.96 × 3.58 to 13.95 μm and 4.24 to 14.01 × 2.4 to 10.86 μm. Genomic DNA was extracted from three isolates and the partial internal transcribed spacer (ITS) regions, intergenic region of apn2 and MAT1-2-1 (ApMAT), and fragments of actin (ACT), glyceraldehydes-3-phosphate dehydrogenase (GAPDH), chitin synthase (CHS-1), and β-tubulin (TUB2) genes were amplified, sequenced, and submitted to GenBank (ITS, ON115173 to ON115175; ApMat, ON156517 to ON156519; ACT, ON146469 to ON146471; GAPDH, ON156502 to ON156504; CHS-1, ON156507 to ON156509; TUB-2, ON156512 to ON156514). A phylogenetic tree was constructed with MrBayes v. 3.2.6 and MEGA v. 10.1.5 based on the concatenation of multiple sequences. The three isolates were grouped with strain Colletotrichum siamense ICMP 18578. Results indicated the three isolates were identified as C. siamense Prihastuti, L. Cai & K.D. Hyde. To confirm the pathogenicity of the three isolates, four sets (five plants per set) of 160 healthy leaves of 2-year-old plants (J. sambac, eight leaves per plant) were slightly scratched with a sterilized toothpick at each of eight locations. Conidial suspensions (1 × 10⁶ conidia/ml) in 0.1% Tween 20 were inoculated onto each wounded spot of three sets as the treatment groups, and wounded leaves treated with sterile water were the control. All plants were covered with plastic bags and cultivated in a phytotron (12 h/12 h light/dark, 28°C). After 7 days, irregular chlorotic regions with brown lesions were observed on inoculated leaves while no symptoms appeared on controls. The same fungi were reisolated from inoculated leaves and confirmed by morphological and molecular identification, fulfilling Koch’s postulates. C. siamense has been associated with leaf anthracnose of J. sambac in Vietnam (Wikee et al. 2011) and Jasminum mesnyi in China (Zhang et al. 2019). To our knowledge, this is the first report of C. siamense causing jasmine anthracnose in China, which provides a reference for the management of this disease.
    Keywords Colletotrichum ; Jasminum sambac ; actin ; anthracnose ; appressoria ; chitin synthase ; conidia ; conidiomata ; culture media ; defoliation ; dieback ; ethanol ; floriculture crops ; fungi ; intergenic DNA ; internal transcribed spacers ; leaf spot ; leaves ; mycelium ; oxidoreductases ; pathogenicity ; phylogeny ; polysorbates ; China ; Vietnam ; Colletotrichum siamense
    Language English
    Dates of publication 2023-0701
    Publishing place The American Phytopathological Society
    Document type Article ; Online
    ZDB-ID 754182-x
    ISSN 0191-2917
    ISSN 0191-2917
    DOI 10.1094/PDIS-07-22-1547-PDN
    Database NAL-Catalogue (AGRICOLA)

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  2. Article: First Report of Colletotrichum siamense Causing Leaf Spot on Jasminum sambac in China.

    Sun, Mingyan / Li, Chunniu / Li, Xianmin / Bu, Zhaoyang / La, Yanfei / Liu, Kedan / Li, Qili

    Plant disease

    2022  

    Abstract: Jasmine (Jasminum sambac (L.) Aiton) is cultivated as a commercial floricultural crop in many countries around the world (Gao et al., 2020). From June to August 2020, leaf spots on jasmine were observed on a jasmine plantation in Hengzhou of Guangxi ... ...

    Abstract Jasmine (Jasminum sambac (L.) Aiton) is cultivated as a commercial floricultural crop in many countries around the world (Gao et al., 2020). From June to August 2020, leaf spots on jasmine were observed on a jasmine plantation in Hengzhou of Guangxi province. Over 40% of the plants in 6 ha fields were infected. This disease was prevalent in jasmine production area of China (Chen et al., 2012; Du et al., 2020). Symptoms began as chlorotic regions (from 5 to 10 mm in diameter) with light brown necrotic centers, which gradually expanded to the entire leaf. Eventually, the disease leaded to defoliation and dieback. The edges of the affected parts from diseased leaves were cut into pieces (3 mm2). Pieces were treated with 75% ethanol for 10 s, soaked in 2% NaClO solution for 1 min, washed three times with sterile water, and then incubated on potato dextrose agar (PDA) plates at 28℃ for 5 days in the dark. Fungal cultures that showed similar morphological characteristics were isolated, and three representative isolates (HL6-1 to HL6-3) were purified following Mo et al. (2018). The cultures on PDA changed from white to dark grey after 7 days and produced conidiomata after 14 days. Conidia were hyaline, one-celled, guttulate, cylindrical, of 12.07 to 18.09 × 4.04 to 8.05 μm, 13.17 to 16.35 × 4.22 to 6.13 μm and 10.11 to 22.17 × 3.65 to 8.1 μm for HL6-1, HL6-2 and HL6-3, respectively. Gray-brown or dark brown appressoria formed from conidia were subglobose or elliptical. Conidial appressoria and mycelial appressoria were 5.53 to 13.96 × 3.58 to 13.95 μm and 4.24 to 14.01 × 2.4 to 10.86 μm. Genomic DNA was extracted from three isolates and the partial internal transcribed spacer (ITS) regions, intergenic region of apn2 and MAT1-2-1 (ApMAT), and fragments of actin (ACT), glyceraldehydes-3-phosphate dehydrogenase (GAPDH), chitin synthase (CHS-1), and β-tubulin (TUB2) genes were amplified, sequenced and submitted to GenBank (ITS, ON115173 to ON115175; ApMat, ON156517 to ON156519; ACT, ON146469 to ON146471; GAPDH, ON156502 to ON156504; CHS-1, ON156507 to ON156509; TUB-2, ON156512 to ON156514). Phylogenetic tree was constructed with MrBayes v. 3.2.6 and MEGA v. 10.1.5 based on the concatenation of multiple sequences. Three isolates were grouped with strain C. siamense ICMP 18578. Results indicated three isolates were identified as Colletotrichum siamense Prihastuti, L. Cai & K.D. Hyde. To confirm the pathogenicity of the three isolates, four sets (five plants per set) of 160 healthy leaves of 2-year-old plants (J. sambac, eight leaves per plant) were slightly scratched with a sterilized toothpick at each of eight locations. Conidial suspension (1×106 conidia/mL) in 0.1% Tween 20 were inoculated onto each wounded spot of three sets as the treatment groups, while wounded leaves treated with sterile water as the control. All plants were covered with plastic bags and cultivated in phytotron (12 h/12 h light/dark, 28°C). After 7 days, irregular chlorotic regions with brown lesions were observed on inoculated leaves while no symptoms on controls. The same fungi were reisolated from inoculated leaves and confirmed by morphological and molecular identification, fulfilling Koch's postulates. Colletotrichum siamense has been associated with leaf anthracnose of J. sambac in Vietnam (Wikee et al., 2011) and J. mesnyi in China (Zhang et al., 2019). To our knowledge, this is the first report of C. siamense causing jasmine anthracnose in China, which provides a reference for the management of this disease.
    Language English
    Publishing date 2022-12-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 754182-x
    ISSN 0191-2917
    ISSN 0191-2917
    DOI 10.1094/PDIS-07-22-1547-PDN
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: WNT7A Overexpression Inhibits Growth and Migration of Hepatocellular Carcinoma via the

    Lan, Lihui / Wang, Wei / Huang, Yue / Zhao, Chenghai / Bu, Xianmin

    BioMed research international

    2019  Volume 2019, Page(s) 3605950

    Abstract: Background/Aims. ...

    Abstract Background/Aims.
    MeSH term(s) Carcinoma, Hepatocellular/metabolism ; Carcinoma, Hepatocellular/pathology ; Cell Movement ; Cell Survival ; Gene Expression Regulation, Neoplastic ; Hep G2 Cells ; Humans ; Liver Neoplasms/metabolism ; Liver Neoplasms/pathology ; Neoplasm Proteins/metabolism ; Wnt Proteins/biosynthesis ; Wnt Signaling Pathway ; beta Catenin/metabolism
    Chemical Substances Neoplasm Proteins ; WNT7A protein, human ; Wnt Proteins ; beta Catenin
    Language English
    Publishing date 2019-11-18
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2698540-8
    ISSN 2314-6141 ; 2314-6133
    ISSN (online) 2314-6141
    ISSN 2314-6133
    DOI 10.1155/2019/3605950
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: MiR-29b inhibits hypertrophic scar tissue inflammation after burn through regulating TGF-β1/Smad signaling pathway.

    Yu, Jing / Zhang, Lian / Zhang, Shuang / Xian, Guangyan / Zhao, Yuping / Bu, Xianmin

    Italian journal of dermatology and venereology

    2019  Volume 156, Issue 2, Page(s) 251–252

    MeSH term(s) Burns ; Cicatrix, Hypertrophic/pathology ; Humans ; Inflammation ; MicroRNAs/genetics ; Signal Transduction ; Transforming Growth Factor beta1/genetics
    Chemical Substances MicroRNAs ; Transforming Growth Factor beta1
    Language English
    Publishing date 2019-09-26
    Publishing country Italy
    Document type Journal Article
    ZDB-ID 3065415-4
    ISSN 2784-8450
    ISSN (online) 2784-8450
    DOI 10.23736/S2784-8671.19.06444-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases.

    Lan, Lihui / Wang, Wei / Huang, Yue / Bu, Xianmin / Zhao, Chenghai

    Journal of cellular biochemistry

    2019  Volume 120, Issue 11, Page(s) 18588–18598

    Abstract: Human Wnt family comprises 19 proteins which are critical to embryo development and tissue homeostasis. Binding to different frizzled (FZD) receptor, Wnt7a initiates both β-catenin dependent pathway, and β-catenin independent pathways such as PI3K/Akt, ... ...

    Abstract Human Wnt family comprises 19 proteins which are critical to embryo development and tissue homeostasis. Binding to different frizzled (FZD) receptor, Wnt7a initiates both β-catenin dependent pathway, and β-catenin independent pathways such as PI3K/Akt, RAC/JNK, and extracellular signal-regulated kinase 5/peroxisome proliferator-activated receptor-γ. In the embryo, Wnt7a plays a crucial role in cerebral cortex development, synapse formation, and central nervous system vasculature formation and maintenance. Wnt7a is also involved in the development of limb and female reproductive system. Wnt7a mutation leads to human limb malformations and animal female reproductive system defects. Wnt7a is implicated in homeostasis maintenance of skeletal muscle, cartilage, cornea and hair follicle, and Wnt7a treatment may be potentially applied in skeletal muscle dystrophy, corneal damage, wound repair, and hair follicle regeneration. Wnt7a plays dual roles in human tumors. Wnt7a is downregulated in lung cancers, functioning as a tumor suppressor, however, it is upregulated in several other malignancies such as ovarian cancer, breast cancer, and glioma, acting as a tumor promoter. Moreover, Wnt7a overexpression is associated with inflammation and fibrosis, but its roles need to be further investigated.
    MeSH term(s) Animals ; Embryonic Development/genetics ; Frizzled Receptors/genetics ; Frizzled Receptors/metabolism ; Genes, Tumor Suppressor ; Homeostasis/genetics ; Humans ; Mutation ; Neoplasms/genetics ; Neoplasms/metabolism ; Protein Binding ; Signal Transduction/genetics ; Wnt Proteins/genetics ; Wnt Proteins/metabolism ; beta Catenin/genetics ; beta Catenin/metabolism
    Chemical Substances CTNNB1 protein, human ; Frizzled Receptors ; WNT7A protein, human ; Wnt Proteins ; beta Catenin
    Language English
    Publishing date 2019-06-29
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 392402-6
    ISSN 1097-4644 ; 0730-2312
    ISSN (online) 1097-4644
    ISSN 0730-2312
    DOI 10.1002/jcb.29217
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: WNT7A Overexpression Inhibits Growth and Migration of Hepatocellular Carcinoma via the β-Catenin Independent Pathway

    Lihui Lan / Wei Wang / Yue Huang / Chenghai Zhao / Xianmin Bu

    BioMed Research International, Vol

    2019  Volume 2019

    Abstract: Background/Aims. Hepatocellular carcinoma (HCC) is the lethal digestive cancer and the second leading cause of cancer death in men worldwide. Wnt7a, a 39Kd secreted glycoprotein composed of 349 amino acids, was reported to be related to various diseases. ...

    Abstract Background/Aims. Hepatocellular carcinoma (HCC) is the lethal digestive cancer and the second leading cause of cancer death in men worldwide. Wnt7a, a 39Kd secreted glycoprotein composed of 349 amino acids, was reported to be related to various diseases. However, its role in HCC has not been studied yet. In this study, using gene expression data and clinical information obtained from the Oncomine and KMplot database, we acknowledged that WNT7A was underexpressed in HCC cancer tissue compared with normal tissue, and WNT7A underexpression was correlated with the decreased survival rate of HCC patients. The function of Wnt7a in cell viability, apoptosis, and migration was evaluated by biological behavior assay and molecular analysis. The findings revealed that WNT7A overexpression significantly restrained cell viability and migration while enhancing apoptosis. In addition, WNT7A overexpression promoted cell apoptosis by strengthening Caspase-3 activity and inhibited migration by downregulating EMT transcriptional factor Snail. Furthermore, the expression level of SKP2 was significantly downregulating in the WNT7A overexpression group. In conclusion, this study illustrated that overexpression of WNT7A inhibited cell viability and migration, which was likely attributed to the regulation of SKP2/P21.
    Keywords Medicine ; R
    Subject code 610
    Language English
    Publishing date 2019-01-01T00:00:00Z
    Publisher Hindawi Limited
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article: Inflammatory myofibroblastic tumor in the head of the pancreas with anorexia and vomiting in a 69-year-old man: A case report.

    Ding, Ding / Bu, Xianmin / Tian, Feng

    Oncology letters

    2016  Volume 12, Issue 2, Page(s) 1546–1550

    Abstract: Inflammatory myofibroblastic tumor (IMT) is a rare condition of unclear etiology that is commonly observed in the lung but rarely in the pancreas. WHO classified IMT as a potentially malignant or aggressive tumor. In the present report, the case of a 69- ... ...

    Abstract Inflammatory myofibroblastic tumor (IMT) is a rare condition of unclear etiology that is commonly observed in the lung but rarely in the pancreas. WHO classified IMT as a potentially malignant or aggressive tumor. In the present report, the case of a 69-year-old male patient with an IMT in the head of the pancreas, who experienced anorexia, nausea and vomiting, is presented. The patient's clinical symptoms were nonspecific, and the imaging findings revealed a hypovascularized pancreatic mass with stenosis of the descending duodenum. The electronic endoscopy findings revealed protruding lesions in the duodenal bulb and the descending duodenum. Biopsies of the mass were conducted with an electronic endoscope, but were not diagnostic. Subsequent duodenopancreatectomy aided in determining a pathological diagnosis of IMT, based on the histology and immunohistochemistry results. The patient experienced a recovery without further incident, as observed during a regular follow-up 3 years later. IMT in the head of the pancreas is rare, particularly in adults. In the present study, an extremely rare case of IMT involving the head of the pancreas in an adult patient is presented, and the therapeutic options for this condition are discussed.
    Language English
    Publishing date 2016-06-28
    Publishing country Greece
    Document type Journal Article
    ZDB-ID 2573196-8
    ISSN 1792-1082 ; 1792-1074
    ISSN (online) 1792-1082
    ISSN 1792-1074
    DOI 10.3892/ol.2016.4787
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Significant association between GSTT1 null genotype and susceptibility to pancreatic cancer.

    Bu, Xianmin / Zhao, Chenghai

    Molecular biology reports

    2013  Volume 40, Issue 7, Page(s) 4295–4299

    Abstract: Many studies have investigated the association between glutathione S-transferase T1 (GSTT1) polymorphism and risk for pancreatic cancer, but those studies have yielded contradictory findings on the association. We performed a comprehensive search in the ... ...

    Abstract Many studies have investigated the association between glutathione S-transferase T1 (GSTT1) polymorphism and risk for pancreatic cancer, but those studies have yielded contradictory findings on the association. We performed a comprehensive search in the PubMed, EMBASE, and the Chinese National Knowledge Infrastructure databases to identify relevant studies. A meta-analysis was performed to examine the association between GSTT1 polymorphism and susceptibility to pancreatic cancer by calculating the pooled odds ratios (ORs) and corresponding 95 % confidence intervals (95 % CIs). Eight studies involving a total of 4,437 individuals were included. Overall, significantly increased pancreatic cancer risk was associated with GSTT1 null genotype when all studies were pooled into the meta-analysis (random effects OR = 1.61, 95 % CI 1.06-2.44; P = 0.025). Significantly increased risk of pancreatic cancer was also found for GSTT1 null genotype in Asians when stratified by ethnicity (fixed effects OR = 2.67, 95 % CI 1.74-4.09; P < 0.001). The findings demonstrate that GSTT1 null genotype have a modest effect on the genetic susceptibility to pancreatic cancer, and GSTT1 null genotype is associated with increased risk of pancreatic cancer.
    MeSH term(s) Genetic Predisposition to Disease ; Genotype ; Glutathione Transferase/genetics ; Humans ; Odds Ratio ; Pancreatic Neoplasms/genetics ; Publication Bias
    Chemical Substances glutathione S-transferase T1 (EC 2.5.1.-) ; Glutathione Transferase (EC 2.5.1.18)
    Language English
    Publishing date 2013-05-30
    Publishing country Netherlands
    Document type Journal Article ; Meta-Analysis ; Research Support, Non-U.S. Gov't
    ZDB-ID 186544-4
    ISSN 1573-4978 ; 0301-4851
    ISSN (online) 1573-4978
    ISSN 0301-4851
    DOI 10.1007/s11033-013-2516-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: The association between cyclooxygenase-2 1195 G/A polymorphism and hepatocellular carcinoma: evidence from a meta-analysis.

    Bu, Xianmin / Zhao, Chenghai

    Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine

    2013  Volume 34, Issue 3, Page(s) 1479–1484

    Abstract: Cyclooxygenase-2 (COX-2) is proven to influence the carcinogenesis through immune response suppression, apoptosis inhibition, angiogenesis regulation, and tumor cell invasion. Previous studies assessing the association between COX-2 1195 G/A polymorphism ...

    Abstract Cyclooxygenase-2 (COX-2) is proven to influence the carcinogenesis through immune response suppression, apoptosis inhibition, angiogenesis regulation, and tumor cell invasion. Previous studies assessing the association between COX-2 1195 G/A polymorphism and susceptibility to hepatocellular carcinoma (HCC) reported conflicting results. The objective of the study was to investigate the association between COX-2 1195 G/A polymorphism and HCC by a meta-analysis. PubMed, Embase, Web of Science, and Wangfang databases were searched for studies investigating the association between COX-2 1195 G/A polymorphism and HCC risk. The pooled odds ratio (OR) and its 95 % confidence interval (CI) were used to assess the strength of the association. Five studies with a total of 1,690 HCC cases and 1,961 controls were identified. Meta-analyses of total included studies showed that there was an obvious association between COX-2 1195 G/A polymorphism and HCC risk under two main genetic models (for AA versus GG, fixed-effects OR=1.45, 95 % CI 1.15-1.81, P=0.001, I (2) =0.0 %; for AA/GA versus GG, fixed-effects OR=1.26, 95 % CI 1.05-1.51, P=0.011, I (2) =0.0 %). Subgroup analysis by ethnicity showed that association was still obvious in Asians under two genetic models (for AA versus GG, fixed-effects OR=1.45, 95 % CI 1.16-1.82, P=0.001, I (2) =21.7 %; for AA/GA versus GG, fixed-effects OR=1.27, 95 % CI 1.05-1.54, P=0.013, I (2) =0.4 %). The evidence from the meta-analysis supports an association between COX-2 1195 G/A polymorphism and HCC risk in Asians. Further studies with large sample and careful design are needed to identify the possible association in Caucasians.
    MeSH term(s) Carcinoma, Hepatocellular/etiology ; Case-Control Studies ; Cyclooxygenase 2/genetics ; Genetic Predisposition to Disease ; Humans ; Liver Neoplasms/etiology ; Polymorphism, Genetic/genetics ; Risk Factors
    Chemical Substances Cyclooxygenase 2 (EC 1.14.99.1) ; PTGS2 protein, human (EC 1.14.99.1)
    Language English
    Publishing date 2013-03-14
    Publishing country Netherlands
    Document type Journal Article ; Meta-Analysis ; Research Support, Non-U.S. Gov't
    ZDB-ID 605825-5
    ISSN 1423-0380 ; 0289-5447 ; 1010-4283
    ISSN (online) 1423-0380
    ISSN 0289-5447 ; 1010-4283
    DOI 10.1007/s13277-013-0672-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Significant association between GSTT1 null genotype and susceptibility to pancreatic cancer

    Bu, Xianmin / Zhao, Chenghai

    Molecular biology reports. 2013 July, v. 40, no. 7

    2013  

    Abstract: Many studies have investigated the association between glutathione S-transferase T1 (GSTT1) polymorphism and risk for pancreatic cancer, but those studies have yielded contradictory findings on the association. We performed a comprehensive search in the ... ...

    Abstract Many studies have investigated the association between glutathione S-transferase T1 (GSTT1) polymorphism and risk for pancreatic cancer, but those studies have yielded contradictory findings on the association. We performed a comprehensive search in the PubMed, EMBASE, and the Chinese National Knowledge Infrastructure databases to identify relevant studies. A meta-analysis was performed to examine the association between GSTT1 polymorphism and susceptibility to pancreatic cancer by calculating the pooled odds ratios (ORs) and corresponding 95 % confidence intervals (95 % CIs). Eight studies involving a total of 4,437 individuals were included. Overall, significantly increased pancreatic cancer risk was associated with GSTT1 null genotype when all studies were pooled into the meta-analysis (random effects OR = 1.61, 95 % CI 1.06–2.44; P = 0.025). Significantly increased risk of pancreatic cancer was also found for GSTT1 null genotype in Asians when stratified by ethnicity (fixed effects OR = 2.67, 95 % CI 1.74–4.09; P < 0.001). The findings demonstrate that GSTT1 null genotype have a modest effect on the genetic susceptibility to pancreatic cancer, and GSTT1 null genotype is associated with increased risk of pancreatic cancer.
    Keywords Asians ; confidence interval ; databases ; genotype ; glutathione transferase ; meta-analysis ; odds ratio ; pancreatic neoplasms ; risk
    Language English
    Dates of publication 2013-07
    Size p. 4295-4299.
    Publishing place Springer-Verlag
    Document type Article
    ZDB-ID 186544-4
    ISSN 1573-4978 ; 0301-4851
    ISSN (online) 1573-4978
    ISSN 0301-4851
    DOI 10.1007/s11033-013-2516-4
    Database NAL-Catalogue (AGRICOLA)

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