5.9
CiteScore
5.9
Impact Factor

2017 Vol. 44, No. 12

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Original research
Migfilin promotes migration and invasion in glioma by driving EGFR and MMP-2 signalings: A positive feedback loop regulation
Yunwei Ou, Qingnan Wu, Chuanyue Wu, Xuefeng Liu, Yongmei Song, Qimin Zhan
2017, 44(12): 557-565. doi: 10.1016/j.jgg.2017.09.008
Abstract (99) HTML PDF (5)
Abstract:
Glioma is the most common type of primary brain tumors in the central nervous system (CNS). Migfilin occurs in human glioma and enhances cellular motility via the epidermal growth factor receptor (EGFR) pathway. However, the underlying molecular mechanism is not fully understood. In this study, we found that Migfilin promoted matrix metalloproteinase-2 (MMP-2) activity, and restrained the expression of tissue inhibitor of metalloproteinase 2 (TIMP2), which is an MMP-2 inhibitor. Functional and structural studies showed that the LIM1 domain of Migfilin was required for Migfilin-mediated TIMP2 expression inhibition and MMP-2 activity, and was also necessary in promoting cell motility. Furthermore, Migfilin-induced EGFR phosphorylation was greatly reduced by MMP-2 inhibitor (GM6001) or siRNA, while Migfilin-induced MMP-2 activation was also blocked by the EGFR inhibitor (AG1478) or siRNA. MMP-2 and EGFR inhibitors and their siRNAs can block Migfilin-induced migration and invasion, respectively. These results demonstrated that EGFR and MMP-2 signalings may form a positive feedback loop to enhance Migfilin-induced migration and invasion. Finally, we detected that the expression of Migfilin, EGFR phosphorylation (Tyr1173) and MMP-2 activity had a positive correlation in the clinical glioma sample. Taken together, these results suggest that Migfilin is a critical regulator in cellular motility by driving the EGFR-MMP-2 feedback loop, and may be considered as a potential therapeutic target in glioma.
Ribosome biogenesis protein Urb1 acts downstream of mTOR complex 1 to modulate digestive organ development in zebrafish
Jia He, Yun Yang, Junren Zhang, Jinzi Chen, Xiangyong Wei, Jianbo He, Lingfei Luo
2017, 44(12): 567-576. doi: 10.1016/j.jgg.2017.09.013
Abstract (144) HTML PDF (9)
Abstract:
Ribosome biogenesis is essential for the cell growth and division. Disruptions in ribosome biogenesis result in developmental defects and a group of diseases, known as ribosomopathies. Here, we report a mutation in zebrafish urb1, which encodes an essential ribosome biogenesis protein. Theurb1 mutant exhibits hypoplastic digestive organs, which is caused by impaired cell proliferation with the differentiation of digestive organ progenitors unaffected. Knockdown of mtor or raptor leads to similar hypoplastic phenotypes and reduced expression of urb1 in the digestive organs. Overexpression of Urb1 results in overgrowth of digestive organs, and can efficiently rescue the hypoplastic liver and pancreas in the mtor and raptor morphants. Reduced syntheses of free ribosomal subunits and impaired assembly of polysomes are observed in the urb1 mutant as well as in the mtor and raptor morphants, which can be rescued by the Urb1 overexpression. These data demonstrate that Urb1 plays an important role in governing ribosome biogenesis and protein synthesis downstream of mammalian/mechanistic target of rapamycin complex 1 (mTORC1), thus regulating the development of digestive organs. Our study indicates the requirement of hyperactive protein synthesis for the digestive organ development.
Essential roles of stat5.1/stat5b in controlling fish somatic growth
Shuting Xiong, Jie Mei, Peipei Huang, Jing Jing, Zhi Li, Jingliang Kang, Jian-Fang Gui
2017, 44(12): 577-585. doi: 10.1016/j.jgg.2017.07.006
Abstract (96) HTML PDF (2)
Abstract:
Signal transducer and activator of transcription 5b (STAT5b) has been identified as a key downstream mediator of growth hormone (GH) signaling in somatic growth of mammalian. However, the corresponding homologue gene of Stat5b is unknown in fish species. In this study, we generated loss-of-function mutants in stat5.1 and stat5.2, two stat5 homologues existing in zebrafish. In stat5.1-deficient zebrafish, a significant reduction of body length and body weight was detected in the embryos/larvae and adults compared with the wild-type control fish, and sexual size dimorphism in adult zebrafish was also eliminated. However, the stat5.2-deficient zebrafish displayed a normal developmental phenotype during all lifespan. Chromatin immunoprecipitation combined with deep sequencing (ChIP-seq) method was adopted to further investigate the potential transcriptional targets of Stat5 protein and cast much light upon the biological function of Stat5. We identified more than 800 genes as transcriptional targets of Stat5 during zebrafish embryogenesis. KEGG analysis indicated that the Stat5 target gene network is predominantly linked to the metabolic pathways, neuroactive ligand-receptor interaction and JAK-STAT signaling pathways. Further validation studies suggested that Stat5.1 protein could directly regulate the expression of gh1, and stat5.1-mutated zebrafish showed a reduction of gh1 mRNA level. In the present study, stat5.1 was revealed as the corresponding homologue gene of Stat5b in fish species. Additionally, we found a novel molecular interaction between Stat5.1/Stat5b and GH, and unraveled a positive feedback loop Stat5.1-GH-Stat5.1 which is necessary for somatic growth and body development in zebrafish.
Letter to the editor
Mediator complex components are frequent targets for genetic alterations in various types of human cancer
Libin Deng, Cheng Zhang, Duling Miao, Xiaoli Tang, Shiwen Luo, Hong-Bo Xin, Huidong Shi
2017, 44(12): 587-591. doi: 10.1016/j.jgg.2017.08.006
Abstract (84) HTML PDF (3)
Abstract:
The role of cystatin A in breast cancer and its functional link with ERα
Dixcy Jaba Sheeba John Mary, Mohan C. Manjegowda, Ajay Kumar, Sarbajeet Dutta, Anil M. Limaye
2017, 44(12): 593-597. doi: 10.1016/j.jgg.2017.10.001
Abstract (142) HTML PDF (4)
Abstract:
Dynamic patterns of gene expression during leaf initiation
Ting Yu, Chunmei Guan, Jin Wang, Muhammad Sajjad, Lingjian Ma, Yuling Jiao
2017, 44(12): 599-601. doi: 10.1016/j.jgg.2017.11.001
Abstract (123) HTML PDF (3)
Abstract: