Jianhua Yang

Dr. Jianhua Yang


Research Focus & Metrics

Academic Career Length

16Years (2011-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 OncoTargets and Therapy
Verified
Journal Article
Open access
PDF file
HYHai-Lan Yu
Hai-Lan Yu
XMXu-Dong Ma
Xu-Dong Ma
JTJin-Fei Tong
Jin-Fei Tong
JLJian-Qiong Li
Jian-Qiong Li
XGXiao-Jing Guan
Xiao-Jing Guan
JYJianhua Yang
Jianhua Yang
Background: The Wilms’ tumor suppressor WT1 is reported to work in a range of physiological processes at both transcriptional and posttranscriptional level. WT1-associating protein (WTAP), a nuclear protein co-localized with splicing factors, also plays a vital role in cellular function and cancer progression. However, little is known about the role of WTAP in ovarian cancer and the underlying mechanism. Materials and methods: To evaluate the expression of WTAP, multiple means were applied in clinical tissues, including immunohistochemistry, quantitative reverse transcriptase PCR (qRT-PCR), and Western blot. Two representative ovarian cancer cell lines (3AO and SKOV3) were used to assess the malignant influence of WTAP on proliferation, apoptosis, and migration. To explore its function, WTAP was additionally down-regulated by lentivirus. Results: High expression of WTAP in high-grade serous ovarian carcinoma (HGSOC) predicted a shorter overall survival (P<0.01). Furthermore, WTAP expression was higher in HGSOC, compared with that in normal ovary group (P<0.01), benign ovarian tumor group (P<0.01), and non-HGSOC group (P<0.05). In HGSOC, high expression of WTAP was significantly related with the lymph node metastasis (P<0.05). In ovarian cancer cell lines, cell proliferation and migration were considerably reduced after WTAP was down-regulated, while apoptotic rate was increased. Moreover, the effect of WTAP in 3AO and SKOV3 might be relevant with MAPK and AKT signaling pathways. Conclusion: WTAP is highly expressed in HGSOC, and indicates a worse survival outcome. Therefore, it is highly possible that WTAP has a prognostic implication in the patients of HGSOC. In addition, WTAP down-regulation also plays a tumor suppressor role in 3AO and SKOV3 cell lines.

23 December 2021 in Frontiers in Endocrinology
Verified
Journal Article
Open access
LJLingling Jiang
Lingling Jiang
HFHaiyi Fei
Haiyi Fei
JTJinfei Tong
Jinfei Tong
JZJiena Zhou
Jiena Zhou
JZJiajuan Zhu
Jiajuan Zhu
SZSongying Zhang
Songying Zhang
Objective: We explored the gut microbiome and serum metabolome alterations in patients with premature ovarian insufficiency (POI) and the effects of hormone replacement therapy (HRT) with the aim to unravel the pathological mechanism underlying POI.Methods: Fecal and serum samples obtained from healthy females (HC, n = 10) and patients with POI treated with (n = 10) or without (n = 10) HRT were analyzed using 16S rRNA gene sequencing and untargeted metabolomics analysis, respectively. Peripheral blood samples were collected to detect serum hormone and cytokine levels. Spearman’s rank correlation was used to evaluate correlations between sex hormones and cytokines and between the gut microbiota and serum metabolites. To further confirm the correlation between Eggerthella and ovarian fibrosis, the mice were inoculated with Eggerthella lenta (E. lenta) through oral gavage.Results: The abundance of genus Eggerthella significantly increased in the fecal samples of patients with POI compared to that observed in the samples of HCs. This increase was reversed in patients with POI treated with HRT. Patients with POI showed significantly altered serum metabolic signatures and increased serum TGF-β1 levels; this increase was reversed by HRT. The abundance of Eggerthella was positively correlated with altered metabolic signatures, which were, in turn, positively correlated with serum TGF-β1 levels in all subjects. Estrogen ameliorated ovarian fibrosis induced by E. lenta in mice.Conclusions: The interactions between the gut microbiota, serum metabolites, and serum TGF-β1 in patients with POI may play a critical role in the development of POI. HRT not only closely mimicked normal ovarian hormone production in patients with POI but also attenuated gut microbiota dysbiosis and imbalance in the levels of serum metabolites and TGF-β1, which are reportedly associated with fibrosis. The findings of this study may pave the way for the development of preventive and curative therapies for patients with POI.

1 July 2019 in Cancer Management and Research
Verified
Journal Article
Open access
PDF file
JTJinfei Tong
Jinfei Tong
XMXudong Ma
Xudong Ma
HYHailan Yu
Hailan Yu
JYJianhua Yang
Jianhua Yang
Cancer is expected to rank as the leading cause of death worldwide due to increasing morbidity and mortality. Long noncoding RNAs (lncRNAs) have been found to play pivotal roles in multiple biological processes, such as transcriptional interference, posttranscriptional regulation and epigenetic modification. Small nucleolar RNA host gene 15 (SNHG15), a snoRNA host gene which produces a short half-lived lncRNA, was reported to be upregulated in tumor cells and participate in the occurrence and development of multiple cancers. And more than half of the SNHG15 research in cancers has been published within the last 2 years. In this review, we summarized the current evidence concerning the biological functions and molecular mechanisms of SNHG15 in various cancers, including gastric, hepatocellular, pancreatic, colorectal, breast, and thyroid cancer, osteosarcoma, glioma, lung cancer, renal cell carcinoma, and epithelial ovarian cancer. SNHG15 plays critical roles in regulation of cell proliferation, migration and invasion of tumors via different potential mechanisms. Moreover, the abnormal expression of SNHG15 was associated with clinical features of patients with cancers. Consequently, SNHG15 could be considered as a promising biomarker for cancer diagnosis, prognosis or treatment.

1 September 2020 in Cancer Management and Research
Verified
Journal Article
Open access
PDF file
JTJinfei Tong
Jinfei Tong
XZXiao Zhang
Xiao Zhang
YFYunlong Fan
Yunlong Fan
LCLingfeng Chen
Lingfeng Chen
XMXudong Ma
Xudong Ma
JYJianhua Yang
Jianhua Yang
Purpose: Ovarian cancer is the leading cause of death in gynecologic malignancies. Growing evidences demonstrate that a complicated relationship exists between the gut microbiota and cancer treatment. However, there are few studies explored the alterations of gut microbiota in ovarian cancer patients following anti-cancer treatments. Therefore, we aim to analyze the changes of the gut microbiota in ovarian cancer patients treated with radical surgery and chemotherapy. Patients and Methods: The microbial genes were examined from a total of 75 fecal samples from 18 ovarian cancer patients, including 10 preoperative fecal samples (Group B), 4 postoperative fecal samples (Group M0), as well as 61 fecal samples after first to fifth cycles of chemotherapy, using 16S rRNA sequencing. Results: Our results showed that fecal samples collected in postoperative (Group M0) exhibited significant decreases in abundance of Bacteroidetes and Firmicutes, while a significant increase in abundance of Proteobacteria compared with preoperative (Group B) fecal samples. LEfSe analysis identified that Bilophila and Faecalibacterium are the key genera in Group B, while Klebsiella and Enterococcus are the key genus in Group M0. Compared with before chemotherapy, the abundance of Bacteroidetes and Firmicutes increased, and the abundance of Proteobacteria decreased after chemotherapy. In addition, anaerobic bacteria, such as Bacteroides, Collinsella and Blautia, exhibited significant increases after chemotherapy. Moreover, we observed that certain bacterial genera were significantly correlated with clinicopathological characteristics of ovarian cancer patients. Conclusion: Our study suggested that radical surgery and chemotherapy altered the composition of gut microbiota in ovarian cancer patients. Therapeutic strategies targeting the gut microbiota may be beneficial for the clinical treatment of ovarian cancer.

26 May 2011 in Archives of Gynecology and Obstetrics
Verified
Journal Article
Closed access
PDF file
JYJianhua Yang
Jianhua Yang
CYChunxiao Yan
Chunxiao Yan
WZWei Zheng
Wei Zheng
XCXuejun Chen
Xuejun Chen

1 February 2021 in Environmental Research Letters
Verified
Journal Article
Open access
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SQShen Qiu
Shen Qiu
LLLeizhen Liu
Leizhen Liu
WZWenhui Zhao
Wenhui Zhao
JYJianhua Yang
Jianhua Yang
XHXinyi Han
Xinyi Han
JWJianjun Wu
Jianjun Wu
Solar-induced chlorophyll fluorescence (SIF) is closely related to vegetation photosynthesis, and is considered as a direct and non-invasive indicator of the functional status of photosynthetic machinery; the normalized difference vegetation index (NDVI) can also reflect photosynthetic characteristics. Both are related to surface soil moisture (SSM), which is susceptible to drought, and phenology plays an important role in these vegetation-moisture relationships. Based on a variety of gridded SIF, NDVI, and SSM datasets obtained from satellite sensors, we presented the detailed relationships of SSM with SIF and NDVI in different phenological stages. Results showed that SIF and NDVI were significantly correlated with SSM in different phenological stages, especially during the maturity and senescence stages. For different vegetation types, SIF was more sensitive than NDVI to SSM anomalies in grasslands and forests during the maturity stage and rainfed croplands during the senescence stage. These relationships were regulated by precipitation and mean temperature, and decreased precipitation had the most significant impact when accompanied by increased temperature during the maturity stage or decreased temperature during the senescence stage. Our findings shed light on the role that phenology has in the relationships of SSM with SIF and NDVI on a large scale, which can further improve the understanding of vegetation-moisture relationships.