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Featured researches published by Man Jiang.


bioRxiv | 2018

Using molecular ecological network analysis to explore the effects of chemotherapy on intestinal microbial communities of colorectal cancer patients

Jing Cong; Jingjuan Zhu; Chuantao Zhang; Tianjun Li; Kewei Liu; Dong Liu; Na Zhou; Man Jiang; Helei Hou; Xiaochun Zhang

Intestinal microbiota is now widely known to be key roles in the nutrition uptake, metabolism, and the regulation of human immune responses. However, we do not know how changes the intestinal microbiota in response to the chemotherapy. In this study, we used network-based analytical approaches to explore the effects of five stages of chemotherapy on the intestinal microbiota of colorectal cancer patients. The results showed that chemotherapy greatly reduced the alpha diversity and changed the specie-specie interaction networks of intestinal microbiota, proved by the network size, network connectivity and modularity. The OTU167 and OTU8 from the genus Fusobacterium and Bacteroides were identified as keystone taxa by molecular ecological networks in the first two stages of chemotherapy, and were significantly correlated with tumor makers (P < 0.05). Five stages of chemotherapy did not make the intestinal micro-ecosystem regain a steady state, because of the lower alpha diversity and more complicated ecological networks compared to the healthy individuals. Furthermore, combing the changes of ecological networks with the tumor markers, the intestinal microbiota was closely linked with clinical chemotherapeutic effects. Importance A deeply understanding of the role of intestinal microbiota contributes to help us find path forward for improving the prognosis of colorectal cancer patients. In addition, diet or probiotics interventions will be a possible attempt to improve the clinical chemotherapeutic effects for colorectal cancer patients.


Oncology Letters | 2018

Apatinib suppresses cell growth and metastasis and promotes antitumor activity of temozolomide in glioma

Chao Wang; Man Jiang; Helei Hou; Qiang Lin; Zhiyong Yan; Xiaochun Zhang

Apatinib, a small-molecule multi-targeted tyrosine kinase inhibitor, is widely used to treat various types of solid tumors. In the present study, it was investigated whether apatinib has therapeutic potential for glioma. Cell Counting Kit-8 and colony formation assays were utilized to determine the cell viability of p53- and EGFR-mutated U251MG glioma cells, and wild-type U-87MG ATCC glioma cells. Furthermore, apoptosis, and the invasion and migration abilities of glioma cells were investigated by flow cytometry, invasion assays and wound-healing assays. The potential of the combination of apatinib with temozolomide (TMZ) for glioma therapy was also investigated. The results demonstrate that apatinib significantly inhibited cell proliferation and colony formation through promoting cell apoptosis in p53- and EGFR-mutated and wild-type glioma cells. Cell invasion and migration abilities were notably decreased following treatment with apatinib. Overall, the present study indicates a synergistic antitumor effect of apatinib and TMZ in glioma, and presents a basis for the use of apatinib in glioma treatment.


Oncologist | 2018

Comprehensive Molecular Characterization of Young Chinese Patients with Lung Adenocarcinoma Identified a Distinctive Genetic Profile

Helei Hou; Hua Zhu; Han Zhao; Weihua Yan; Yongjie Wang; Man Jiang; Bin Liu; Dong Liu; Na Zhou; Chuantao Zhang; Pansong Li; Lianpeng Chang; Yanfang Guan; Zhe Wang; Xiaoping Zhang; Zhuokun Li; Bingliang Fang; Xiaochun Zhang

BACKGROUNDnOccurrence at a younger age has been demonstrated to be associated with a distinct biology in non-small cell lung cancer. However, genomics and clinical characteristics among younger patients with lung adenocarcinoma remain to be determined. Here we studied the potentially targetable genetic alterations by next-generation sequencing (NGS) assay in young Chinese patients with lung adenocarcinoma.nnnMATERIALS AND METHODSnSeventy-one surgically resected lung adenocarcinoma tissue samples from patients aged less than 45 years were collected with informed consent from all patients. Targeted NGS assays were used to identify actionable genetic alterations in the cancer tissues. Additionally, the genomic and clinicopathologic characteristics of 106 patients with lung adenocarcinoma who received NGS testing over the same period were analyzed retrospectively.nnnRESULTSnThe frequencies of targetable genetic alterations in 177 patients with lung adenocarcinoma were analyzed by defined age categories, which unveiled a distinctive molecular profile in the younger group, aged less than 45 years. Notably, higher frequency of ALK and HER2 genetic alterations were associated with young age. However, a reverse trend was observed for KRAS, STK11 and EGFR exon 20 mutations, which were more frequently identified in the older group, aged more than 46 years. Furthermore, concurrent EGFR/TP53 mutations were much more prevalent in the younger patients (81.6% vs. 46.8%), which might have a poor response to treatment with epidermal growth factor receptor tyrosine kinase inhibitor.nnnCONCLUSIONnIn this study, NGS assay revealed a distinctive genetic profile in younger patients with adenocarcinoma. High frequency of concurrent EGFR/TP53 mutations was found in the younger patients, which especially warranted personalized treatment in this population.nnnIMPLICATIONS FOR PRACTICEnFurther investigation is needed to understand the genomics and clinical characteristics of young patients with lung adenocarcinoma. In the present study, hybrid capture-based next-generation sequencing assays were used to identify targeted genetic alterations in young lung adenocarcinoma patients. Young patients with lung adenocarcinoma, aged less than 45 years, harbored a higher frequency of ALK and HER2 genetic alterations compared with patients aged more than 46 years. Dramatically, concurrent EGFR/TP53 mutations were much more prevalent in younger patients, which had a poor response to treatment with epidermal growth factor receptor kinase inhibitor. These results reveal a distinctive genetic profile in younger patients with adenocarcinoma, which might improve the treatment of this subpopulation.


Oncologist | 2018

Concordance Study Between IBM Watson for Oncology and Clinical Practice for Patients with Cancer in China

Na Zhou; Chuantao Zhang; Hongying Lv; Chen‐Xing Hao; Tianjun Li; Jingjuan Zhu; Hua Zhu; Man Jiang; K. Liu; Helei Hou; Dong Liu; Ai‐Qin Li; Guo‐Qing Zhang; Zi‐Bin Tian; Xiaochun Zhang

BACKGROUNDnIBM Watson for Oncology (WFO), which can use natural language processing to evaluate data in structured and unstructured formats, has begun to be used in China. It provides physicians with evidence-based treatment options and ranks them in three categories for treatment decision support. This study was designed to examine the concordance between the treatment recommendation proposed by WFO and actual clinical decisions by oncologists in our cancer center, which would reflect the differences of cancer treatment between China and the U.S.nnnPATIENTS AND METHODSnRetrospective data from 362 patients with cancer were ingested into WFO from April 2017 to October 2017. WFO recommendations were provided in three categories: recommended, for consideration, and not recommended. Concordance was analyzed by comparing the treatment decisions proposed by WFO with those of the multidisciplinary tumor board. Concordance was achieved when the oncologists treatment decisions were in the recommended or for consideration categories in WFO.nnnRESULTSnOvarian cancer showed the highest concordance, which was 96%. Lung cancer and breast cancer obtained a concordance of slightly above 80%. The concordance of rectal cancer was 74%, whereas colon cancer and cervical cancer showed the same concordance of 64%. In particular, the concordance of gastric cancer was very low, only 12%, and 88% of cases were under physicians choice.nnnCONCLUSIONnDifferent cancer types showed different concordances, and only gastric cancers were significantly less likely to be concordant. Incidence and pharmaceuticals may be the major cause of discordance. To be comprehensively and rapidly applied in China, WFO needs to accelerate localization. ClinicalTrials.gov Identifier: NCT03400514.nnnIMPLICATIONS FOR PRACTICEnIBM Watson for Oncology (WFO) has begun to be used in China. In this study, concordance was examined between the treatment recommendation proposed by WFO and clinical decisions for 362 patients in our cancer center, which could reflect the differences of cancer treatment between China and the U.S. Different cancer types showed different concordances, and only gastric cancers were significantly less likely to be concordant. Incidence and pharmaceuticals may be the major causes of discordance. To be comprehensively and rapidly applied in China, WFO needs to accelerate localization. This study may have a significant effect on application of artificial intelligence systems in China.


Journal of Thoracic Oncology | 2017

P1.01-069 Clinical Experience with IBM Watson for Oncology (WFO) Cognitive System for Lung Cancer Treatment in China

Na Zhou; Hongying Lv; Chuantao Zhang; Tianjun Li; Jingjuan Zhu; Man Jiang; Helei Hou; Dong Liu; A. Li; G. Liu; K. Liu; G. Zhang; Xiaochun Zhang


Journal of Clinical Oncology | 2018

Apatinib in combination with S-1 as first-line treatment in patients with advanced gastric cancer: A phase II clinical trial.

Chuantao Zhang; Zimin Liu; Na Zhou; Jianli Zhang; Jingjuan Zhu; Hongying Lv; Tianjun Li; Helei Hou; Dong Liu; Jing Cong; Man Jiang; K. Liu; Zhumei Cui; Yanbing Zhou; Xiaochun Zhang


Journal of Thoracic Oncology | 2017

P3.03-018 Tumor Cavitation in Lung Metastases in Patients with Solid Tumor Treated with Apatinib

Man Jiang; Na Zhou; Dong Liu; Helei Hou; Jing Cong; Chuantao Zhang; Zhang X


Journal of Thoracic Oncology | 2017

P2.03-034 EGFR Exon 19 Deletion Is Associated with Favorable Overall Survival After First-Line Icotinib Therapy in Advanced NSCLC Patients

Chuantao Zhang; Helei Hou; X. Cheng; D. Gong; Hong Liu; H. Yu; W. Zhu; Jingjuan Zhu; K. Liu; Hongying Lv; Na Zhou; Jing Cong; Dong Liu; L. Yang; Man Jiang; Y. Zhang; Lijuan Chen; Y. Zhu; Zhang X


Journal of Thoracic Oncology | 2017

P3.03-014 Tumor Cavitation in Patients with Primary Lung Cancer Following Apatinib Treatment

Man Jiang; Na Zhou; H. Zhu; Chuantao Zhang; Hongying Lv; Jingjuan Zhu; Tianjun Li; K. Liu; Zhang X


Journal of Thoracic Oncology | 2017

P1.01-042 Dynamic ctDNA Assay by Next Generation Sequencing to Guide Targeted Therapy in Advanced Non-Small Cell Lung Cancer

Dong Liu; Helei Hou; Na Zhou; Man Jiang; Jing Cong; Chuantao Zhang; Tianjun Li; Hongying Lv; Jingjuan Zhu; C. Hao; K. Liu; Xiaochun Zhang

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