Bin Li

Dr. Bin Li


Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

View All Publications
1 January 2014 in Oxidative Medicine and Cellular Longevity
Verified
Journal Article
Open access
PDF file
SLSiying Li
Siying Li
WWWenjuan Wang
Wenjuan Wang
TNTing Niu
Ting Niu
HWHui Wang
Hui Wang
BLBin Li
Bin Li
Taixing CuiTaixing Cui
Taixing Cui
The anticancer therapy of doxorubicin (Dox) has been limited by its acute and chronic cardiotoxicity. In addition to a causative role of oxidative stress, autophagy appears to play an important role in the regulation of Dox-induced cardiotoxicity. However, the underlying mechanisms remain unclear. Accordingly, we explored a role of nuclear factor erythroid-2 related factor 2 (Nrf2) in Dox-induced cardiomyopathy with a focus on myocardial oxidative stress and autophagic activity. In wild type (WT) mice, a single intraperitoneal injection of 25 mg/kg Dox rapidly induced cardiomyocyte necrosis and cardiac dysfunction, which were associated with oxidative stress, impaired autophagy, and accumulated polyubiquitinated protein aggregates. However, these Dox-induced adverse effects were exaggerated in Nrf2 knockout (Nrf2−/−) mice. In cultured cardiomyocytes, overexpression of Nrf2 increased the steady levels of LC3-II, ameliorated Dox-induced impairment of autophagic flux and accumulation of ubiquitinated protein aggregates, and suppressed Dox-induced cytotoxicity, whereas knockdown of Nrf2 exerted opposite effects. Moreover, the exaggerated adverse effects in Dox-intoxicated Nrf2 depleted cardiomyocytes were dramatically attenuated by forced activation of autophagy via overexpression of autophagy related gene 5 (Atg5). Thus, these results suggest that Nrf2 is likely an endogenous suppressor of Dox-induced cardiotoxicity by controlling both oxidative stress and autophagy in the heart.

21 September 2013 in BMC Biotechnology
Verified
Journal Article
Open access
PDF file
BLBin Li
Bin Li
ZWZemin Wang
Zemin Wang
SLShiwu Li
Shiwu Li
WDWilliam Donelan
William Donelan
XWXingli Wang
Xingli Wang
DTDongqi Tang
Dongqi Tang
Background: Lactose intolerance is a common health concern causing gastrointestinal symptoms and avoidance of dairy products by afflicted individuals. Since milk is a primary source of calcium and vitamin D, lactose intolerant individuals often obtain insufficient amounts of these nutrients which may lead to adverse health outcomes. Production of lactose-free milk can provide a solution to this problem, although it requires use of lactase from microbial sources and increases potential for contamination. Use of thermostable lactase enzymes can overcome this issue by functioning under pasteurization conditions. Results: A thermostable β-glucosidase gene from Pyrococcus furiosus was cloned in frame with the Saccharomyces cerecisiae a-factor secretory signal and expressed in Pichia pastoris strain X-33. The recombinant enzyme was purified by a one-step method of weak anion exchange chromatography. The optimum temperature and pH for this β-glucosidase activity was 100°C and pH 6.0, respectively. The enzyme activity was not significantly inhibited by Ca2+. We tested the additive amount, hydrolysis time, and the influence of glucose on the enzyme during pasteurization and found that the enzyme possessed a high level of lactose hydrolysis in milk that was not obviously influenced by glucose. Conclusions: The thermostablity of this recombinant β-glucosidase, combined with its neutral pH activity and favorable temperature activity optima, suggest that this enzyme is an ideal candidate for the hydrolysis of lactose in milk, and it would be suitable for application in low-lactose milk production during pasteurization.

29 May 2020 in BMC Endocrine Disorders
Verified
Journal Article
Open access
PDF file
RHRui-Ting Hu
Rui-Ting Hu
DLDe-Shan Liu
De-Shan Liu
BLBin Li
Bin Li
Background: Radioactive iodine (RAI) therapy is an important treatment option for Graves’ disease (GD), the main side effect of RAI treatment is hypothyroidism, and the factors resulting in hypothyroidism are still controversial. The purpose of this retrospective study was to clarify the possible risk factors of early hypothyroidism after RAI therapy in Graves’ disease.Methods: We reviewed 312 GD patients treated with RAI between January 2017 to December 2018, collected the potential risk factors, and analyzed the relationship between these variables and early hypothyroidism.Results: After 6 months’ follow-up, 218 (69.87%) patients were evaluated as early hypothyroid. Male gender, shorter duration of disease, smaller thyroid weight, lower 2-h radioactive iodine uptake (RAIU), 6-h RAIU, 24-h RAIU and 6/24-h uptake ratio, lower administered dosages were significantly associated with early hypothyroidism. Logistics regression analysis showed that male gender, smaller thyroid weight and lower 6-h RAIU were associated with early hypothyroidism. Multi-factors combined ROC curve analysis suggested that the predictive power of male gender, smaller thyroid weight and lower 6-h RAIU for early hypothyroidism was 0.711.Conclusions: Our results show that RAI is an effective therapy for GD and most of the cured patients became to hypothyroid within 6 months. Male gender, smaller thyroid weight and lower 6-h RAIU are the main risk factors for early hypothyroidism.

1 February 2014 in Biochemical and Biophysical Research Communications
Verified
Journal Article
Closed access
BLBin Li
Bin Li
AAAkram Abdalrahman
Akram Abdalrahman
YLYimu Lai
Yimu Lai
JJJoseph S. Janicki
Joseph S. Janicki
KWKeith W. Ward
Keith W. Ward
Taixing CuiTaixing Cui
Taixing Cui

24 March 2014 in PLOS ONE
Verified
Journal Article
Open access
PDF file
YLYongqiang Li
Yongqiang Li
ZCZhou Chaomin
Zhou Chaomin
XSXiaofei Shao
Xiaofei Shao
Xinyu LiuXinyu Liu
Xinyu Liu
Jia GuoJia Guo
Jia Guo
HZHequn Zou
Hequn Zou
To examine the relationship between the HW phenotype and risk for CKD in a community population aged 40 years and older. A cross-sectional study was conducted in Zhuhai from June to October 2012. The participants were divided into three groups: Group 1, Waist circumference >90 cm in men or >85 cm in women and triglycerides ≥2 mmol/l; Group 3, Waist circumference ≤90 cm in men or ≤85 cm in women and triglycerides <2 mmol/l; Group 2, The remaining participants. The prevalence of the three subgroups and CKD were determined. The association between HW phenotype and CKD was then analyzed using SPSS (version 13.0). After adjusting for age and sex, Group 1 was associated with CKD (OR 3.08, 95% CI 2.01, 4.73, P<0.001), when compared with Group 3. Further adjustment for factors which were potential confounders and unlikely to be in the causal pathway between the HW phenotype and CKD, Group 1 was still significantly associated with CKD. The OR for CKD was 2.65 (95% CI 1.65, 4.26, P<0.001). When adjusted for diabetes and hypertension, the association of Group 1 and CKD was still significant (OR 2.09, 95% CI 1.26, 3.45, P = 0.004). Group 2 was associated with CKD (OR 1.81, 95% CI 1.29, 2.53, P = 0.001), when compared with Group 3. Further adjustment for factors which were potential confounders, Group 2 was still significantly associated with CKD. The OR for CKD was 1.75 (95% CI 1.22, 2.51, P = 0.002). When adjusted for diabetes and hypertension, the association between Group 2 and CKD still existed. The OR for CKD was 1.48 (95% CI 1.01, 2.16, P = 0.046). Our results showed that HW phenotype was associated with CKD in the population aged 40 years and older.

26 August 2025 in Medical Science Monitor
Verified
Journal Article
Open access
RHRui-Ting Hu
Rui-Ting Hu
BLBin Li
Bin Li
BACKGROUND The aim of this study was to determine the remission rate and factors influencing radioactive iodine (RAI) therapy in pediatric patients with Graves' hyperthyroidism (GH) who received treatment for the first time. MATERIAL AND METHODS This retrospective study analyzed a total of 44 pediatric patients with GH who received their first RAI therapy in the nuclear treatment ward of Linyi People's Hospital from December 2018 to December 2023. Follow-up was conducted for 6 months after treatment, and based on treatment outcomes, the patients were divided into the remission group and the failure group. SPSS 22.0 statistical software was used to compare and analyze the predictive factors between the 2 groups. RESULTS The total remission rate of GH at 6 months after RAI therapy was 52.3% (23/44). There were significant differences between the remission group and the failure group in terms of duration of GH, thyroid weight, and RAI dose. Logistic regression analysis indicated that duration of GH and thyroid weight were the factors influencing remission of RAI therapy. Patients with a duration of GH more than 27 months and a thyroid weight greater than 50.17g were less likely to be cured. CONCLUSIONS The disease duration and thyroid weight influenced the RAI therapy outcome in pediatric patients with GH. Higher doses of RAI should be administered to patients with a disease duration exceeding 27 months or thyroid weight surpassing 50.17 g.