Lan Li

Dr. Lan 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

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4 January 2014 in Molecular Biology Reports
Verified
Journal Article
Closed access
PDF file
LLLan Li
Lan Li
TZTeng Zhang
Teng Zhang
XQXunsi Qin
Xunsi Qin
WGWei Ge
Wei Ge
HMHua-Gang Ma
Hua-Gang Ma
ZXZhang Xi-Feng
Zhang Xi-Feng

1 June 2015 in PLOS ONE
Verified
Journal Article
Open access
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XQXunsi Qin
Xunsi Qin
MCMingjun Cao
Mingjun Cao
FLFangnong Lai
Fangnong Lai
FYFan Yang
Fan Yang
WGWei Ge
Wei Ge
LLLan Li
Lan Li
Oxidative stress (OS), as a signal of aberrant intracellular mechanisms, plays key roles in maintaining homeostasis for organisms. The occurrence of OS due to the disorder of normal cellular redox balance indicates the overproduction of reactive oxygen species (ROS) and/or deficiency of antioxidants. Once the balance is broken down, repression of oxidative stress is one of the most effective ways to alleviate it. Ongoing studies provide remarkable evidence that oxidative stress is involved in reproductive toxicity induced by various stimuli, such as environmental toxicants and food toxicity. Zearalenone (ZEA), as a toxic compound existing in contaminated food products, is found to induce mycotoxicosis that has a significant impact on the reproduction of domestic animals, especially pigs. However, there is no information about how ROS and oxidative stress is involved in the influence of ZEA on porcine granulosa cells, or whether the stress can be rescued by curcumin. In this study, ZEA-induced effect on porcine granulosa cells was investigated at low concentrations (15 μM, 30 μM and 60 μM). In vitro ROS levels, the mRNA level and activity of superoxide dismutase, glutathione peroxidase and catalase were obtained. The results showed that in comparison with negative control, ZEA increased oxidative stress with higher ROS levels, reduced the expression and activity of antioxidative enzymes, increased the intensity of fluorogenic probes 2’, 7’-Dichlorodihydrofluorescin diacetate and dihydroethidium in flow cytometry assay and fluorescence microscopy. Meanwhile, the activity of glutathione (GSH) did not change obviously following 60 μM ZEA treatment. Furthermore, the underlying protective mechanisms of curcumin on the ZEA-treated porcine granulosa cells were investigated. The data revealed that curcumin pre-treatment significantly suppressed ZEA-induced oxidative stress. Collectively, porcine granulosa cells were sensitive to ZEA, which may induce oxidative stress. The findings from this study clearly demonstrate that curcumin is effective to reduce the dysregulation of cellular redox balance on porcine granulosa cells in vitro and should be further investigated for its protective role against ZEA in animals.

1 January 2018 in International Journal of Biological Sciences
Verified
Journal Article
Open access
XLXue-Lian Liu
Xue-Lian Liu
RWRui-Ying Wu
Rui-Ying Wu
XSXiao-Feng Sun
Xiao-Feng Sun
SCShun-Feng Cheng
Shun-Feng Cheng
RZRui-Qian Zhang
Rui-Qian Zhang
LLLan Li
Lan Li
Zearalenone (ZEA), a metabolite of Fusarium fungi, is commonly found on moldy grains. Because it can competitively combine to estrogen receptor to disrupt estrogenic signaling, it has been reported to have serious adverse effects on animal reproduction systems. In order to explore the genotoxic effects of ZEA exposure on ovarian somatic cells, porcine granulosa cells were exposed to 10 μM and 30 μM ZEA for 24 or 72 h in vitro. The results showed that ZEA exposure for 24 h remarkably reduced the proliferation of porcine granulosa cells in a dose-dependent manner as determined by MTT analysis and flow cytometry. Furthermore, exposure to ZEA for 72 h induced apoptosis, and RNA sequence analysis also revealed that the expression of apoptosis related genes were altered. RT-qPCR, immunofluorescence and western blot analysis further confirmed the expression of DNA damage and repair related genes (γ-H2AX, BRCA1, RAD51 and PRKDC) were increased in ZEA exposed granulosa cells. When the estrogen antagonist, tamoxifen, was added with ZEA in the culture medium, the DNA damage and repairment by ZEA returned to normal level. Collectively, these results illustrate that ZEA disrupts genome stability and inhibits growth of porcine granulosa cells via the estrogen receptors which may promote granulosa cell apoptosis when the DNA repair system is not enough to rescue this serious damage.

16 January 2014 in Molecular Biology Reports
Verified
Journal Article
Closed access
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CCChun-Lei Chen
Chun-Lei Chen
XFXia-Fei Fu
Xia-Fei Fu
LWLin-Qing Wang
Lin-Qing Wang
JWJun-Jie Wang
Jun-Jie Wang
HMHua-Gang Ma
Hua-Gang Ma
LLLan Li
Lan Li

1 February 2017 in Toxicology and Applied Pharmacology
Verified
Journal Article
Closed access
GZGuo-Liang Zhang
Guo-Liang Zhang
XSXiao-Feng Sun
Xiao-Feng Sun
YFYan-Zhong Feng
Yan-Zhong Feng
BLBo Li
Bo Li
YLYa-Peng Li
Ya-Peng Li
LLLan Li
Lan Li

1 August 2017 in Toxicology and Applied Pharmacology
Verified
Journal Article
Closed access
KLKe-Han Liu
Ke-Han Liu
XSXiao-Feng Sun
Xiao-Feng Sun
YFYan-Zhong Feng
Yan-Zhong Feng
SCShun-Feng Cheng
Shun-Feng Cheng
BLBo Li
Bo Li
LLLan Li
Lan Li