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Featured researches published by Jiping Wang.


Journal of Clinical Oncology | 2011

Plasma MicroRNA Panel to Diagnose Hepatitis B Virus–Related Hepatocellular Carcinoma

Jian Zhou; Lei Yu; Xue Gao; Jie Hu; Jiping Wang; Zhi Dai; Jiefei Wang; Zhiyong Zhang; Shaohua Lu; Xiaowu Huang; Zheng Wang; Shuang-Jian Qiu; Xiao-Ying Wang; Guo-Huan Yang; Hui-Chuan Sun; Zhao-You Tang; Ying Wu; Hongguang Zhu; Jia Fan

PURPOSEnMore than 60% of patients with hepatocellular carcinoma (HCC) do not receive curative therapy as a result of late clinical presentation and diagnosis. We aimed to identify plasma microRNAs for diagnosing hepatitis B virus (HBV) -related HCC.nnnPATIENTS AND METHODSnPlasma microRNA expression was investigated with three independent cohorts including 934 participants (healthy, chronic hepatitis B, cirrhosis, and HBV-related HCC), recruited between August 2008 and June 2010. First, we used microarray to screen 723 microRNAs in 137 plasma samples for diagnosing HCC. Quantitative reverse-transcriptase polymerase chain reaction assay was then applied to evaluate the expression of selected microRNAs. A logistic regression model was constructed using a training cohort (n = 407) and then validated using an independent cohort (n = 390). Area under the receiver operating characteristic curve (AUC) was used to evaluate diagnostic accuracy.nnnRESULTSnWe identified a microRNA panel (miR-122, miR-192, miR-21, miR-223, miR-26a, miR-27a and miR-801) that provided a high diagnostic accuracy of HCC (AUC = 0.864 and 0.888 for training and validation data set, respectively). The satisfactory diagnostic performance of the microRNA panel persisted regardless of disease status (AUCs for Barcelona Clinic Liver Cancer stages 0, A, B, and C were 0.888, 0.888, 0.901, and 0.881, respectively). The microRNA panel can also differentiate HCC from healthy (AUC = 0.941), chronic hepatitis B (AUC = 0.842), and cirrhosis (AUC = 0.884), respectively.nnnCONCLUSIONnWe found a plasma microRNA panel that has considerable clinical value in diagnosing early-stage HCC. Thus, patients who would have otherwise missed the curative treatment window can benefit from optimal therapy.


The American Journal of Gastroenterology | 2004

Paroxetine to treat irritable bowel syndrome not responding to high-fiber diet: a double-blind, placebo-controlled trial.

Gary Tabas; Mary Beaves; Jiping Wang; Paul Friday; Houssam Mardini; George L. Arnold

OBJECTIVE:The purpose of the trial was to determine whether a high-fiber diet (HFD) alone or in combination with paroxetine or placebo was effective treatment for patients with irritable bowel syndrome (IBS).METHODS:Design: Trial of HFD alone (Group 1) followed by a randomized, double-blind trial of HFD with paroxetine or placebo (Group 2). Setting: Gastroenterology office in a 524-bed university-affiliated community hospital in Pittsburgh. Patients: Men and women, aged 18–65 yr, previously diagnosed with IBS but otherwise healthy. Intervention: Institution of HFD in 98 participants consuming low- or average-fiber diets. Allocation of paroxetine to 38 and placebo to 43 symptomatic participants consuming HFDs. Measurements: Overall well-being, abdominal pain, and abdominal bloating (Groups 1 and 2); food avoidance, work functioning, and social functioning (Group 2).RESULTS:In Group 1, overall well-being improved in 26% patients, and abdominal pain and bloating decreased in 22% and 26% patients, respectively, with an HFD. In Group 2, overall well-being improved more with paroxetine than with placebo (63.3%vs 26.3%; p= 0.01), but abdominal pain, bloating, and social functioning did not. With paroxetine, food avoidance decreased (p = 0.03) and work functioning was marginally better (p = 0.08). Before unblinding, more paroxetine recipients than placebo recipients wanted to continue their study medication (84%vs 37%; p < 0.001).CONCLUSIONS:The difference in overall well-being found in our paroxetine/placebo trial is greater than that found in previously published drug/placebo trials for IBS. Moreover, the difference in well-being applied to nondepressed recipients of paroxetine.


Annals of Surgical Oncology | 2008

Lymph Node Ratio: Role in the Staging of Node-Positive Colon Cancer

Jiping Wang; James M. Hassett; Merril T. Dayton; Mahmoud N. Kulaylat

AbstractBackgroundRecent literature has shown that lymph node ratio (LNR) is superior to the number of positive lymph nodes (pLNs) in predicting the prognosis in several malignances other than colon cancer. We hypothesize that LNR may play a similar role in stage III colon cancer.MethodsWe included 24,477 stage III colon cancer cases from the Surveillance, Epidemiology, and End Results cancer registry. Patients were categorized into four groups, LNR1 to 4, according to cutoff points n


Annals of Surgery | 2012

Comparison of a lymph node ratio-based staging system with the 7th AJCC system for gastric cancer: analysis of 18,043 patients from the SEER database.

Jiping Wang; Ping Dang; Chandrajit P. Raut; Prakash K. Pandalai; Ugwuji N. Maduekwe; David W. Rattner; Gregory Y. Lauwers; Sam S. Yoon


Annals of Surgery | 2010

Should total number of lymph nodes be used as a quality of care measure for stage III colon cancer

Jiping Wang; Mahmoud N. Kulaylat; Howard Rockette; James M. Hassett; Ashwani Rajput; Kelli Bullard Dunn; Merril T. Dayton

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Journal of Gastrointestinal Surgery | 2008

The Prognostic Superiority of Log Odds of Positive Lymph Nodes in Stage III Colon Cancer

Jiping Wang; James M. Hassett; Merril T. Dayton; Mahmoud N. Kulaylat

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American Journal of Clinical Oncology | 2009

Wide excision or Mohs micrographic surgery for the treatment of primary dermatofibrosarcoma protuberans.

Ari-Nareg Meguerditchian; Jiping Wang; Bethany Lema; William G. Kraybill; Nathalie C. Zeitouni; John M. Kane

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Journal of General Internal Medicine | 2008

Patients with Depression are at Increased Risk for Secondary Cardiovascular Events after Lower Extremity Revascularization

Gregory S. Cherr; Pamela M. Zimmerman; Jiping Wang; Hasan H. Dosluoglu

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Clinical Cancer Research | 2014

Functional Genetic Approach Identifies MET, HER3, IGF1R, INSR Pathways as Determinants of Lapatinib Unresponsiveness in HER2-Positive Gastric Cancer

Zhe Zhang; Jiping Wang; Dongmei Ji; Chenchen Wang; Rujiao Liu; Zheng Wu; Lian Liu; Dan Zhu; Jinjia Chang; Ruixuan Geng; Lei Xiong; Qiangyi Fang; Jin Li

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Annals of Surgical Oncology | 2015

Comparison of Gastric Cancer Survival Between Caucasian and Asian Patients Treated in the United States: Results from the Surveillance Epidemiology and End Results (SEER) Database

Jiping Wang; Yihong Sun; Monica M. Bertagnolli

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C. J. Xiao

Chinese Academy of Sciences

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Chandrajit P. Raut

Brigham and Women's Hospital

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X.-D. Wang

Chinese Academy of Sciences

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