|
|
Expression and clinical pathological significance of SOX11 in glioblastoma |
WU Jing LI Xiaojie HE Jie |
Department of Pathology, Anhui Provincial Cancer Hospital, Anhui Province, Hefei 230031, China |
|
|
Abstract Objective To investigate the expression and clinical pathological significance of SOX11 in glioblastoma. Methods A total of 264 cases of paraffin-embedded glioblastoma were collected from the Department of Pathology, Anhui Provincial Hospital from September 2010 to January 2017. Each sample was selected from the tumor area and the normal brain tissue of the tumor to make tissue chips. The expression of SOX11 was detected by immunohistochemistry and the relationship between SOX11 expression and clinicopathological features was analyzed. Results The total positive rate and strongly positive rate of SOX11 expression in glioblastoma was significantly higher than that in matched normal tissues of the tumor (P < 0.01). The expression of SOX11 was correlated with tumor diameter and Ki67 proliferation index (P < 0.01), but it was not related to the patient′s age, gender, single/multiple lesions (P > 0.05). Conclusion SOX11 is specifically expressed in glioblastoma and can be used as a marker for the pathological diagnosis of glioblastoma. The expression level of SOX11 may be related to tumor progression.
|
|
|
|
|
[1] Balta EA,Schaffner I,Wittmann MT,et al. Phosphorylation of the neurogenic transcription factor SOX11 on serine 133 modulates neuronal morphogenesis [J]. Sci Rep,2018, 8(1):16 196.
[2] Narayan C,Kumar A. Constitutive over expression of IL-1β,IL-6,NF-κB,and Stat3 is a potential cause of lung tumorgenesis in urethane (ethyl carbamate) induced Balb/c mice [J]. J Carcinog,2012,11:9.
[3] Szostakowska M,Szymczyk M,Badowska K,et al. SOX11 expression as a MRD molecular marker for MCL in comparison with t(11;14) and IGH rearrangement [J]. Med Oncol,2018,35(4):49.
[4] Xu S,Dong Y,Huo Z,et al. SOX11:a potentially useful marker in surgical pathology:a systematic analysis of SOX11 expression in epithelial and non-epithelial tumours [J]. Histopathology,2019,74(3):391-405.
[5] Zhang S,Chen X,Wang M,et al. Genome-wide identification,phylogeny and expressional profile of the Sox gene family in channel catfish (Ictalurus punctatus) [J]. Comp Bio-chem Physiol Part D Genomics Proteomics,2018,28:17-26.
[6] Khan U,Study D,Baker E,et al. Observation of Cleft Palate in an Individual with SOX11 Mutation: Indication of a Role for SOX11 in Human Palatogenesis [J]. Cleft Palate Craniofac J,2018,55(3):456-461.
[7] Sock E,Rettig SD,Enderich J,et al. Gene targeting reveals a widespread role for the high-mobility-group transcription factor Sox11 in tissue remodeling [J]. Mol Cell Biol,2004,24(15):6635-6644.
[8] Zawerton A,Yao B,Yeager JP,et al. De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism [J]. Am J Hum Genet,2019,104(4):777.
factor in mantle cell lymphoma [J]. Curr Opin Hematol,2018,25(4):299-306.
[9] Jankowski MP,Miller L,Koerber HR. Increased Expression of Transcription Factor SRY-box-Containing Gene 11 (Sox11) Enhances Neurite Growth by Regulating Neurotrophic Factor Responsiveness [J]. Neuroscience,2018, 382:93-104.
[10] Turan S,Boerstler T,Kavyanifar A,et al. A novel human stem cell model for Coffin-Siris Syndrome like syndrome reveals the importance of SOX11 dosage for neuronal differentiation and survival [J]. Hum Mol Genet,2019,pii:ddz089. doi:10.1093/hmg/ddz089.
[11] Guttula PK,Agarwal A,Maharana U,et al. Prediction of novel pluripotent proteins involved in reprogramming of male Germline stem cells (GSCs) into multipotent adult Germline stem cells (maGSCs) by network analysis [J]. Comput Biol Chem,2018,76:302-309.
[12] Bergsland M,Werme M,Malewicz M,et al. The establishment of neuronal properties is controlled by Sox4 and Sox11 [J]. Genes Dev,2006,20(24):3475-3486.
[13] Kuo PY,Jatiani SS,Rahman AH,et al. SOX11 augments BCR signaling to drive MCL-like tumor development [J]. Blood,2018,131(20):2247-2255.
[14] Beekman R,Amador V,Campo E. SOX11,a key oncogenic factor in mantle cell lymphoma [J]. Curr Opin Hematol,2018,25(4):299-306.
[15] Aukema SM,Hoster E,Rosenwald A,et al. Expression of TP53 is associated with the outcome of MCL independent of MIPI and Ki-67 in trials of the European MCL Network [J]. Blood,2018,131(4):417-420.
[16] Chang L,Yuan Z,Shi H,et al. miR-145 targets the SOX11 3′UTR to suppress endometrial cancer growth [J]. Am J Cancer Res,2017,7(11):2305-2317.
[17] Wu Z,Huang W,Wang X,et al. Circular RNA CEP128 acts as a sponge of miR-145-5p in promoting the bladder cancer progression via regulating SOX11[J]. Mol Med,2018,24(1):40.
[18] Pugongchai A,Bychkov A,Sampatanukul P. Promoter hypermethylation of SOX11 correlates with adverse clinicopathological features of human prostate cancer [J]. Int J Exp Pathol,2017,98(6):341-346.
[19] Huang J,Ji EH,Zhao X,et al. Sox11 promotes head and neck cancer progression via the regulation of SDCCAG8 [J]. J Exp Clin Cancer Res,2019,38(1):138.
[20] Liu Z,Zhong Y,Chen YJ,et al. SOX11 regulates apoptosis and cell cycle in hepatocellular carcinoma via Wnt/beta-catenin signaling pathway [J]. Biotechnol Appl Biochem,2019,66(2):240-246.
[21] Fu JQ,Chen Z,Hu YJ,et al. A single factor induces neuronal differentiation to suppress glioma cell growth [J]. CNS Neurosci Ther,2019,25(4):486-495.
[22] Camacho-Urkaray E,Santos-Juanes J,Gutierrez-Corres FB,et al. Establishing cut-off points with clinical relevance for bcl-2,cyclin D1,p16,p21,p27,p53,Sox11 and WT1 expression in glioblastoma - a short report [J]. Cell Oncol (Dordr),2018,41(2):213-221. |
|
|
|