Cargando…

CHST2-mediated sulfation of MECA79 antigens is critical for breast cancer cell migration and metastasis

Snail is a denoted transcriptional repressor that plays key roles in epithelial-mesenchymal transition (EMT) and metastasis. Lately, a plethora of genes can be induced by stable expression of Snail in multiple cell lines. However, the biological roles of these upregulated genes are largely elusive....

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhang, Dan, Zhang, Yihong, Zou, Xiuqun, Li, Mengying, Zhang, Hui, Du, Yaning, Wang, Jiamin, Peng, Chicheng, Dong, Chunyan, Hou, Zhaoyuan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126008/ https://www.ncbi.nlm.nih.gov/pubmed/37095090 http://dx.doi.org/10.1038/s41419-023-05797-x

Ejemplares similares

GATA zinc finger protein p66β promotes breast cancer cell migration by acting as a co-activator of Snail
por: Zou, Xiuqun, et al.
Publicado: (2023)

p66α Suppresses Breast Cancer Cell Growth and Migration by Acting as Co-Activator of p53
por: Zhang, Qun, et al.
Publicado: (2021)

Sulfation-dependent recognition of high endothelial venules (HEV)- ligands by L-selectin and MECA 79, and adhesion-blocking monoclonal antibody
Publicado: (1994)

CHST4 might promote the malignancy of cholangiocarcinoma
por: Zhang, Guanran, et al.
Publicado: (2022)

L-Selectin Ligands That Are O-glycoprotease Resistant and Distinct from MECA-79 Antigen are Sufficient for Tethering and Rolling of Lymphocytes on Human High Endothelial Venules
por: Clark, Rachael A., et al.
Publicado: (1998)

Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6
por: Yaylacioglu Tuncay, Fulya, et al.
Publicado: (2016)

Testosterone Decreases the Number of Implanting Embryos, Expression of Pinopode and L-selectin Ligand (MECA-79) in the Endometrium of Early Pregnant Rats
por: Mokhtar, Mohd Helmy, et al.
Publicado: (2020)

Otological Features of Patients with Musculocontractural Ehlers–Danlos Syndrome Caused by Pathogenic Variants in CHST14 (mcEDS-CHST14)
por: Kawakita, Masayuki, et al.
Publicado: (2023)

CHST7 Methylation Status Related to the Proliferation and Differentiation of Pituitary Adenomas
por: Dong, Wei, et al.
Publicado: (2022)

Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)
por: Minatogawa, Mari, et al.
Publicado: (2022)

MECA : mejora de la calidad de los antimicrobianos : recomendaciones SEQ /
Publicado: (2006)

In Vivo Regulation of Steroid Hormones by the Chst10 Sulfotransferase in Mouse
por: Suzuki-Anekoji, Misa, et al.
Publicado: (2013)

CHST11 gene expression and DNA methylation in breast cancer
por: HERMAN, DAMIR, et al.
Publicado: (2015)

Dentro de la Meca Inside Mecca /
Publicado: (2008)

Immunophenotypes of macular corneal dystrophy in India and correlation with mutations in CHST6
por: Sultana, Afia, et al.
Publicado: (2009)

Novel mutations of CHST6 in Iranian patients with macular corneal dystrophy
por: Birgani, Shiva Akbari, et al.
Publicado: (2009)

Detailed Courses and Pathological Findings of Colonic Perforation without Diverticula in Sisters with Musculocontractural Ehlers–Danlos Syndrome Caused by Pathogenic Variant in CHST14 (mcEDS-CHST14)
por: Kobayashi, Tomoko, et al.
Publicado: (2023)

A comprehensive evaluation of 181 reported CHST6 variants in patients with macular corneal dystrophy
por: Zhang, Jing, et al.
Publicado: (2019)

CHST9 rs1436904 genetic variant contributes to prognosis of triple-negative breast cancer
por: Yuan, Jupeng, et al.
Publicado: (2017)

De la Ceca a La Meca
por: Goytisolo, Juan 1931-
Publicado: (1997)

Chondroitin sulfates play a major role in breast cancer metastasis: a role for CSPG4 and CHST11 gene expression in forming surface P-selectin ligands in aggressive breast cancer cells
por: Cooney, Craig A, et al.
Publicado: (2011)

CHST15 promotes the proliferation of TE-1 cells via multiple pathways in esophageal cancer
por: Wang, Xin, et al.
Publicado: (2020)

CHST6 mutation screening and endoplasmatic reticulum stress in macular corneal dystrophy
por: Wang, Liyuan, et al.
Publicado: (2017)

CHST15 gene germline mutation is associated with the development of familial myeloproliferative neoplasms and higher transformation risk
por: Chen, Yi, et al.
Publicado: (2022)

Impact of the Stringent Stress Response on the Expression of Methicillin Resistance in Staphylococcaceae Strains Carrying mecA, mecA1 and mecC
por: Milheiriço, Catarina, et al.
Publicado: (2022)

A potential role of transposon IS431 in the loss of mecA gene
por: Wang, Aihua, et al.
Publicado: (2017)

Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities
por: Zhou, Yuan-Yuan, et al.
Publicado: (2022)

Macular corneal dystrophy in a Chinese family related with novel mutations of CHST6
por: Dang, Xiuhong, et al.
Publicado: (2009)

Functional Characterization of the Osteoarthritis Susceptibility Mapping to CHST11—A Bioinformatics and Molecular Study
por: Reynard, Louise N., et al.
Publicado: (2016)

Transcriptome analysis of tumor-derived mesenchymal progenitor cells shows that CHST15 is a fibrosis regulator of retroperitoneal liposarcoma
por: Sun, Yang, et al.
Publicado: (2022)

Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family
por: Carstens, Nadia, et al.
Publicado: (2016)

Impairments of mecA gene detection in bovine Staphylococcus spp.
por: de Melo, Dayanne Araújo, et al.
Publicado: (2014)

Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds
por: Kausar, Mehran, et al.
Publicado: (2022)

ACAN, MDFI, and CHST1 as Candidate Genes in Gastric Cancer: A Comprehensive Insilco Analysis
por: Vafaeie, Farzane, et al.
Publicado: (2022)

Aging-Associated Changes in Cognition, Expression and Epigenetic Regulation of Chondroitin 6-Sulfotransferase Chst3
por: Baidoe-Ansah, David, et al.
Publicado: (2022)

A Case of Korean Patient with Macular Corneal Dystrophy Associated with Novel Mutation in the CHST6 Gene
por: Lee, You Kyung, et al.
Publicado: (2013)

MRSA Harboring mecA Variant Gene mecC, France
por: Laurent, Frederic, et al.
Publicado: (2012)

Systemic Analysis of the mecA Gene Using a Bioinformatics Tool
por: Tsai, Shin-Yi, et al.
Publicado: (2017)

Investigation of the urbanization contribution to the COVID-19 outbreak in Iran and the MECA countries
por: Bijari, Nikta Bahman, et al.
Publicado: (2021)

SNP Scanning in mecA Gene for Methicillin-Resistant Staphylococcus aureus
por: Salehi, Mitra, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_1nasqambliah6ilkv9se06dec0