chao lin

Dr. chao lin

orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2019 in Radiotherapy and Oncology
Verified
Journal Article
Closed access
SLSai-Lan Liu
Sai-Lan Liu
XSXue-Song Sun
Xue-Song Sun
JYJin-Jie Yan
Jin-Jie Yan
QCQiuyan Chen
Qiuyan Chen
XHXin Hua
Xin Hua
HMHAIQIANG MAI
HAIQIANG MAI

8 July 2019 in BMC Surgery
Verified
Journal Article
Open access
PDF file
CPCheng Peng
Cheng Peng
DZDi Zhou
Di Zhou
LMLingjun Meng
Lingjun Meng
YCYanlong Cao
Yanlong Cao
HZHanwen Zhang
Hanwen Zhang
CLchao lin
chao lin
Although pancreaticoduodenectomy with vein resection (PDVR) is widely performed in selected patients with indications, its benefits remain controversial. In this meta-analysis, we evaluate the safety and efficacy of PDVR in comparison to standard pancreaticoduodenectomy (PD). We searched PubMed, Embase, and Cochrane as well as the Chinese National Knowledge Infrastructure, Weipu, and Wanfang databases for studies that evaluate the value of PVDR. The data of the patients who underwent PD or PDVR were analyzed using Review Manager and STATA software. In comparison with the PD group, the PDVR group had a lower R0 resection rate and higher rates of complications such as biliary fistula, reoperation rate, delayed gastric emptying, cardiopulmonary abnormalities, hemorrhage, in-hospital mortality, 30-day mortality. The blood loss, duration of operation, total hospital stay is higher in PDVR group. Compared to standard PD, PDVR was associated with a greater risk of some specific complications and increase the mortality rate, total hospital stay time, combine with vein resection have a lower R0 resection rate. Therefore, combine with vascular resection for pancreatic cancer needs to be carefully selected by the surgeon.

3 June 2019 in Journal of Translational Medicine
Verified
Journal Article
Open access
PDF file
WWWen Wen
Wen Wen
SMShijuan Mai
Shijuan Mai
XHXin Hua
Xin Hua
MZMei-Yin Zhang
Mei-Yin Zhang
Jialing HuangJialing Huang
Jialing Huang
LGLing Guo
Ling Guo
Early diagnosis is critical to reduce the mortality caused by nasopharyngeal carcinoma (NPC). MicroRNAs (miRNAs) are dysregulated and play important roles in carcinogenesis. Therefore, this study aimed to identify diagnostically relevant circulating miRNA signatures in patients with NPC. Total RNA was extracted from whole blood samples obtained from 120 patients with NPC, 30 patients with head-neck tumors (HNT), and 30 healthy subjects (HSs), and examined by using a custom microarray. The expression levels of four miRNAs identified by using the microarray were validated with quantitative real-time reverse transcription polymerase chain reaction. The 120 patients with NPC and 30 HSs were randomly assigned to training group-1 and validation group-1, respectively. By using significance analysis of microarray (SAM), the specific miRNA expression profiles in whole blood from patients with NPC are obtained. By using lasso regression and adaptive boosting, a diagnostic signature was identified in training group-1, and its accuracy was verified in validation group-1. By using the same methods, another signature to distinguish patients with NPC from those with HNT and HSs was identified in training group-2 and confirmed in validation group-2. There were 117 differentially expressed miRNAs (upregulated and downregulated fold change ≥ 1.5) between the patients with NPC and HSs, among which an 8-miRNA signature was identified with 96.43% sensitivity and 100% specificity [area under the curve (AUC) = 0.995] to diagnose NPC in training group-1 and 86.11% sensitivity and 88.89% specificity (AUC = 0.941) in validation group-1. Compared with traditional Epstein–Barr virus (EBV) seromarkers, this signature was more specific for NPC. Furthermore, a 16-miRNA signature to differentiate NPC from HNT and HS (HNT-HS) was established from 164 differentially expressed miRNAs, which diagnosed NPC and HNT-HS with 100% accuracy (AUC = 1.000) in training group-2 and 87.04% (AUC = 0.924) in validation group-2. The present study identified two miRNA signatures for the highly accurate diagnosis and differential diagnosis of patients with NPC from HSs and patients with HNT. The identified miRNAs might represent novel serological biomarkers and potential therapeutic targets for NPC.

29 March 2019 in Cancer Communications
Verified
Journal Article
Open access
PDF file
SLSai‐Lan Liu
Sai‐Lan Liu
XSXue‐Song Sun
Xue‐Song Sun
XLXiao‐Yun Li
Xiao‐Yun Li
LTLin-Quan Tang
Lin-Quan Tang
QCQiuyan Chen
Qiuyan Chen
HMHAIQIANG MAI
HAIQIANG MAI
Background: Currently, the diagnosis and treatment of nasopharyngeal carcinoma (NPC) patients with residual cervical lymphadenopathy following radical radiotherapy with or without chemotherapy are challenging. We investigated the prognosis of NPC patients with residual cervical lymphadenopathy and assessed the diagnostic and prognostic values of Epstein‐Barr virus (EBV) DNA in these patients. Methods: This study included 82 NPC patients who were diagnosed with suspected residual cervical lymphadenopathy following completion of antitumor therapy. Their plasma EBV DNA levels were measured using quantitative polymerase chain reaction (qPCR) before the initiation of treatment and before neck dissection. Fine needle aspiration cytology (FNAC) was performed in 21 patients. All patients had undergone neck dissection and postoperative pathological examination to identify the nature of residual cervical lymphadenopathy. The overall survival (OS), progression‐free survival (PFS), distant metastasis‐free survival (DMFS), and locoregional relapse‐free survival (LRRFS) were calculated using the Kaplan–Meier method and compared using the log‐rank test. The Cox proportional hazards model was used to calculate hazard ratios (HRs) with 95% confidence intervals (CIs). Multivariable analysis was used to estimate the effect of potential prognostic factors on survival. Results: Following a median follow‐up of 52.6 months, compared with patients with negative postoperative pathological findings for residual cervical lymphadenopathy, the patients with positive findings had a significantly lower 3‐year PFS rate (49.9% vs. 83.3%, P = 0.008). Among NPC patients with residual cervical lymphadenopathy, the patients with preoperative plasma EBV DNA > 0 copy/mL had a lower 3‐year PFS rate than did those with no detectable EBV DNA (43.7% vs. 61.1%, P = 0.031). In addition, combining FNAC with preoperative EBV DNA detection improved the diagnostic sensitivity. Multivariable analysis demonstrated that residual cervical lymphadenopathy with positive postoperative pathological result was an independent prognostic factor for PFS and that detectable preoperative plasma EBV DNA was an independent prognostic factor for OS. Conclusions: Using FNAC combined with preoperative EBV DNA detection improves the sensitivity in diagnosing NPC with residual cervical lymphadenopathy. Compared with patients with undetectable EBV DNA, patients with detectable preoperative plasma EBV DNA have worse prognosis and may require a more aggressive treatment strategy.

28 January 2020 in Journal of Physiology and Biochemistry
Verified
Journal Article
Closed access
PDF file
YXYien Xiang
Yien Xiang
YYYongsheng Yang
Yongsheng Yang
CLchao lin
chao lin
JWJiacheng Wu
Jiacheng Wu
JWjun wu
jun wu

3 July 2020 in Journal of Physiology and Biochemistry
Verified
Journal Article
Closed access
PDF file
CLchao lin
chao lin
YXYien Xiang
Yien Xiang
JSJiyao Sheng
Jiyao Sheng
SLShui Liu
Shui Liu
MCMengying Cui
Mengying Cui
JWjun wu
jun wu