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Journal articles on the topic 'MTDH'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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1

Pei, Guoqing, Meng Luo, Xiaochun Ni, et al. "Autophagy Facilitates Metadherin-Induced Chemotherapy Resistance Through the AMPK/ATG5 Pathway in Gastric Cancer." Cellular Physiology and Biochemistry 46, no. 2 (2018): 847–59. http://dx.doi.org/10.1159/000488742.

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Background/Aims: Metadherin (MTDH) is overexpressed in some malignancies and enhances drug resistance; however, its role in gastric cancer (GC) and the underlying mechanisms remain largely unexplored. Here, we explore the mechanism by which MTDH induces drug resistance in GC. Methods: We analysed the level of MTDH in GC and adjacent normal gastric mucosal tissues by real-time quantitative PCR (q-PCR). We also analysed the level of autophagy by western blot analysis, confocal microscopy, and transmission electron microscopy after MTDH knockdown and overexpression, and examined fluorouracil (5-F

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2

Tong, Liping, Chao Wang, Xuebin Hu, et al. "Correlated overexpression of metadherin and SND1 in glioma cells." Biological Chemistry 397, no. 1 (2016): 57–65. http://dx.doi.org/10.1515/hsz-2015-0174.

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Abstract Glioma is the most common primary brain tumor with poor prognosis. Effective treatment of glioma remains a big challenge due to complex pathogenic mechanisms. Previous studies have shown that metadherin (MTDH) and its interacting protein staphylococcal nuclease domain containing 1 (SND1) are overexpressed in many solid tumors. To elucidate the role of MDTH and SND1 in the pathogenesis of glioma, we examined the expression of MTDH and SND1 in primary glioma tissues and found that both MTDH and SND1 were highly expressed, with similar expression patterns. Co-expression of MTDH and SND1

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3

Li, Peipei, Xin Wang, Chen Na, et al. "Metaherin Contributes To The Pathogenesis Of Chronic Lymohcytic Leukemia." Blood 122, no. 21 (2013): 4130. http://dx.doi.org/10.1182/blood.v122.21.4130.4130.

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Abstract Introduction Dysregulation of proliferation and apoptosis is associated the pathogenesis of CLL. More recently, Metadherin (MTDH) involved in aberrant proliferation, survival, and increased migration, invasiveness, and metastasis of tumor cells, has been demonstrated as a potential crucial mediator of various types of huamn malignancies. MTDH promotes tumor progression by modulating multiple oncogenic signaling pathways (NF-kB, PI3K/Akt and Wnt/beta-catenin). However, there is no report about the role of MTDH in CLL. Since Wnt signaling pathway had been proven to be unusual activated

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4

Ge, Xueling, Xiao Lv, Peipei Li, and Xin Wang. "Overexpression of Metadherin in the Pathogenesis of Diffuse Large B-Cell Lymphoma,." Blood 118, no. 21 (2011): 3653. http://dx.doi.org/10.1182/blood.v118.21.3653.3653.

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Abstract Abstract 3653 Introduction: Diffuse large-B-cell lymphoma (DLBCL) is an aggressive malignancy of mature B lymphocytes with variable biological and cytogenetic features, as well as clinical outcomes. Further investigating specific biomarkers and cellular signaling pathways, understanding molecular pathogenesis of DLBCL and developing more targeted and effective treatments are indispensable for significantly increasing the survival and alleviating the suffering of patients. Metadherin (MTDH) has been demonstrated as a potentially crucial mediator of various types of human malignancies.

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5

Zhu, Kai, Yuanfei Peng, Jinwu Hu та ін. "Metadherin–PRMT5 complex enhances the metastasis of hepatocellular carcinoma through the WNT–β-catenin signaling pathway". Carcinogenesis 41, № 2 (2019): 130–38. http://dx.doi.org/10.1093/carcin/bgz065.

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Abstract Accumulating data suggest that metadherin (MTDH) may function as an oncogene. Our previous study showed that MTDH promotes hepatocellular carcinoma (HCC) metastasis via the epithelial-mesenchymal transition. In this study, we aim to further elucidate how MTDH promotes HCC metastasis. Using Co-immunoprecipitation (co-IP) and mass spectrometry, we found that MTDH can specifically bind to protein arginine methyltransferase 5 (PRMT5). Further functional assays revealed that PRMT5 overexpression promoted the proliferation and motility of HCC cells and that knockout of PRMT5 impeded the eff

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6

Rong, Chunhong, Yanfen Shi, Jun Huang та ін. "The Effect of Metadherin on NF-κB Activation and Downstream Genes in Ovarian Cancer". Cell Transplantation 29 (1 січня 2020): 096368972090550. http://dx.doi.org/10.1177/0963689720905506.

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Ovarian cancer (OC) is the most aggressive gynecological cancer. Even with the advances in detection and therapeutics, it still remains clinically challenging and there is a pressing need to identify novel therapeutic strategies. In searching for rational molecular targets, we identified metadherin (MTDH), a multifunctional gene associated with several tumor types but previously unrecognized in OC. In this study, we found the MTDH is overexpressed in OC tissues. Through in vitro assays with overexpression cells, we characterized the role of MTDH. We confirmed MTDH stable overexpression signifi

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7

Stoop, Johan M. H., and Hans Mooibroek. "Cloning and Characterization of NADP-Mannitol Dehydrogenase cDNA from the Button Mushroom, Agaricus bisporus, and Its Expression in Response to NaCl Stress." Applied and Environmental Microbiology 64, no. 12 (1998): 4689–96. http://dx.doi.org/10.1128/aem.64.12.4689-4696.1998.

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ABSTRACT Mannitol, a six-carbon sugar alcohol, is the main storage carbon in the button mushroom, Agaricus bisporus. Given the physiological importance of mannitol metabolism in growth, fruit body development, and salt tolerance of A. bisporus, the enzyme responsible for mannitol biosynthesis, NADP-dependent mannitol dehydrogenase (MtDH) (EC 1.1.1.138 ), was purified to homogeneity, andMtDH cDNA was cloned, sequenced, and characterized. To our knowledge, this represents the first report on the isolation of a cDNA encoding an NADP-dependent mannitol dehydrogenase. TheMtDH cDNA contains an open

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8

Lai, Trang Huyen, Mahmoud Ahmed, Jin Seok Hwang, et al. "Transcriptional Repression of Raf Kinase Inhibitory Protein Gene by Metadherin during Cancer Progression." International Journal of Molecular Sciences 22, no. 6 (2021): 3052. http://dx.doi.org/10.3390/ijms22063052.

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Raf kinase inhibitory protein (RKIP), also known as a phosphatidylethanolamine-binding protein 1 (PEBP1), functions as a tumor suppressor and regulates several signaling pathways, including ERK and NF-κκB. RKIP is severely downregulated in human malignant cancers, indicating a functional association with cancer metastasis and poor prognosis. The transcription regulation of RKIP gene in human cancers is not well understood. In this study, we suggested a possible transcription mechanism for the regulation of RKIP in human cancer cells. We found that Metadherin (MTDH) significantly repressed the

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9

Nguyen, Yen Thi-Kim, Jeong Yong Moon, Meran Keshawa Ediriweera, and Somi Kim Cho. "Phenethyl Isothiocyanate Suppresses Stemness in the Chemo- and Radio-Resistant Triple-Negative Breast Cancer Cell Line MDA-MB-231/IR Via Downregulation of Metadherin." Cancers 12, no. 2 (2020): 268. http://dx.doi.org/10.3390/cancers12020268.

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Resistance to chemotherapy and radiation therapy is considered a major therapeutic barrier in breast cancer. Cancer stem cells (CSCs) play a prominent role in chemo and radiotherapy resistance. The established chemo and radio-resistant triple-negative breast cancer (TNBC) cell line MDA-MB-231/IR displays greater CSC characteristics than the parental MDA-MB-231 cells. Escalating evidence demonstrates that metadherin (MTDH) is associated with a number of cancer signaling pathways as well as breast cancer therapy resistance, making it an attractive therapeutic target. Kaplan–Meier plot analysis r

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10

Wang, Fang. "miR-384 targets metadherin gene to suppress growth, migration, and invasion of gastric cancer cells." Journal of International Medical Research 47, no. 2 (2019): 926–35. http://dx.doi.org/10.1177/0300060518817171.

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Objective MicroRNA-384 (miR-384) has been reported to function as a tumor suppressor in multiple cancers; however, its role in gastric cancer (GC) remains unclear. Methods We measured expression levels of miR-384 in GC cell lines and in a normal gastric cell line (GES-1). The association between miR-384 and the metadherin gene ( MTDH) was assessed by luciferase reporter assay and western blot. The effects of the miR-384/MTDH axis on GC cell behaviors were measured by CCK-8, wound-healing, and transwell invasion assays. Results miR-384 was significantly downregulated in GC cell lines compared w

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11

Chu, Pei-Yi, Shin-Mae Wang, Po-Ming Chen, Feng-Yao Tang, and En-Pei Isabel Chiang. "Expression of MTDH and IL-10 Is an Independent Predictor of Worse Prognosis in ER-Negative or PR-Negative Breast Cancer Patients." Journal of Clinical Medicine 9, no. 10 (2020): 3153. http://dx.doi.org/10.3390/jcm9103153.

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(1) Background: Tumor hypoxia leads to metastasis and certain immune responses, and interferes with normal biological functions. It also affects glucose intake, down-regulates oxidative phosphorylation, and inhibits fatty-acid desaturation regulated by hypoxia-inducible factor 1α (HIF-1α). Although tumor hypoxia has been found to promote tumor metastasis, the roles of HIF-1α-regulated genes and their application are not completely integrated in clinical practice. (2) Methods: We examined the correlation between HIF-1α, metadherin (MTDH), and interleukin (IL)-10 mRNA expression, as well as thei

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12

Liu, Chunyan, Anne Bordeaux, Stanka Hettich, and Suhui Han. "MicroRNA-497-5p Functions as a Modulator of Apoptosis by Regulating Metadherin in Ovarian Cancer." Cell Transplantation 29 (January 1, 2020): 096368971989706. http://dx.doi.org/10.1177/0963689719897061.

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Ovarian cancer (OC) has a high mortality rate among women worldwide. However, even with the advances in detection and therapeutics, the number of cases is increasing worldwide. Increasingly, microRNAs (miRNAs), including miR-497-5p, have been implicated in the progression of many cancers, but the role of miR-497-5p in OC remains unknown. The purpose of this study was to investigate the underlying molecular mechanism of miR-497-5p in OC. Herein, we find that miR-497-5p is down-regulated in OC tissues, and overexpression of miR-497-5p enhances apoptosis in OC cells. The increased apoptosis was c

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13

Blanco, Mario Andres, Maša Alečković, Yuling Hua, et al. "Identification of Staphylococcal Nuclease Domain-containing 1 (SND1) as a Metadherin-interacting Protein with Metastasis-promoting Functions." Journal of Biological Chemistry 286, no. 22 (2011): 19982–92. http://dx.doi.org/10.1074/jbc.m111.240077.

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Metastasis is the deadliest and most poorly understood feature of malignant diseases. Recent work has shown that Metadherin (MTDH) is overexpressed in over 40% of breast cancer patients and promotes metastasis and chemoresistance in experimental models of breast cancer progression. Here we applied mass spectrometry-based screen to identify staphylococcal nuclease domain-containing 1 (SND1) as a candidate MTDH-interacting protein. After confirming the interaction between SND1 and MTDH, we tested the role of SND1 in breast cancer and found that it strongly promotes lung metastasis. SND1 was furt

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14

Baygi, Modjtaba Emadi, and Parvaneh Nikpour. "Deregulation of MTDH Gene Expression in Gastric Cancer." Asian Pacific Journal of Cancer Prevention 13, no. 6 (2012): 2833–36. http://dx.doi.org/10.7314/apjcp.2012.13.6.2833.

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15

Tong, Liping, Ming Chu, Bingqing Yan, et al. "MTDH promotes glioma invasion through regulating miR-130b-ceRNAs." Oncotarget 8, no. 11 (2017): 17738–49. http://dx.doi.org/10.18632/oncotarget.14717.

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16

Hao, Jin-yan, Yi-ling Yang, Fang-fang Liu, et al. "MTDH expression in invasive micropapillary carcinoma of the breast." Clinical Oncology and Cancer Research 8, no. 2 (2011): 114–19. http://dx.doi.org/10.1007/s11805-011-0568-6.

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17

Diab, Sami, Matei P. Socoteanu, Carlos A. Encarnacion, et al. "High-risk breast cancer genes at 8q22-24 and their role in over 5,000 patients evaluated with the 70-gene risk of recurrence assay." Journal of Clinical Oncology 38, no. 15_suppl (2020): 3569. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.3569.

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3569 Background: Previous studies have shown that CCNE2 expression is higher in patients’ cancers resistant to CDK4/6 inhibitors. Increased expression of CCNE2, MTDH, or TSPYL5, genes contained within the 70-gene risk of distant recurrence signature (70GS), has also been implicated in breast oncogenesis, poor prognosis, and chemoresistance. These genes are located on chromosome region 8q22.1, one of the most recurrently amplified regions out of all 70GS genes in breast tumors (Fatima et al. 2017). MYC, located on 8q24, is overexpressed in 40% of all breast cancers (BC). Here we examined the ex

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18

Peng, Fenfen, Hongyu Li, Shuting Li, et al. "Micheliolide ameliorates renal fibrosis by suppressing the Mtdh/BMP/MAPK pathway." Laboratory Investigation 99, no. 8 (2019): 1092–106. http://dx.doi.org/10.1038/s41374-019-0245-6.

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19

Zhang, Daobao, Zhiyong Liu, Niandong Zheng, Honggang Wu, Zhao Zhang, and Jianguo Xu. "MiR-30b-5p modulates glioma cell proliferation by direct targeting MTDH." Saudi Journal of Biological Sciences 25, no. 5 (2018): 947–52. http://dx.doi.org/10.1016/j.sjbs.2018.02.015.

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20

Qian, Benjiang, Yi Yao, Changming Liu, Jiabing Zhang, Huihong Chen, and Huizhang Li. "SU6668 modulates prostate cancer progression by downregulating MTDH/AKT signaling pathway." International Journal of Oncology 50, no. 5 (2017): 1601–11. http://dx.doi.org/10.3892/ijo.2017.3926.

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21

El-Ashmawy, Nahla E., Enas A. El-Zamarany, Eman G. Khedr, and Mariam A. Abo-Saif. "Effect of modification of MTDH gene expression on colorectal cancer aggressiveness." Gene 698 (May 2019): 92–99. http://dx.doi.org/10.1016/j.gene.2019.02.069.

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22

Vorholt, Julia A., Marina G. Kalyuzhnaya, Christoph H. Hagemeier, Mary E. Lidstrom, and Ludmila Chistoserdova. "MtdC, a Novel Class of Methylene Tetrahydromethanopterin Dehydrogenases." Journal of Bacteriology 187, no. 17 (2005): 6069–74. http://dx.doi.org/10.1128/jb.187.17.6069-6074.2005.

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ABSTRACT Novel methylene tetrahydromethanopterin (H4MPT) dehydrogenase enzymes, named MtdC, were purified after expressing in Escherichia coli genes from, respectively, Gemmata sp. strain Wa1-1 and environmental DNA originating from unidentified microbial species. The MtdC enzymes were shown to possess high affinities for methylene-H4MPT and NADP but low affinities for methylene tetrahydrofolate or NAD. The substrate range and the kinetic properties revealed by MtdC enzymes distinguish them from the previously characterized bacterial methylene-H4MPT dehydrogenases, MtdA and MtdB. While reveali

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23

Meng, Xiangbing, Eric Devor, Shujie Yang, Brandon Schickling, and Kimberly Leslie. "Role of MTDH, FOXM1 and microRNAs in Drug Resistance in Hepatocellular Carcinoma." Diseases 2, no. 3 (2014): 209–25. http://dx.doi.org/10.3390/diseases2030209.

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24

Kannan, Nagarajan, and Connie J. Eaves. "Tipping the Balance: MTDH-SND1 Curbs Oncogene-Induced Apoptosis and Promotes Tumorigenesis." Cell Stem Cell 15, no. 2 (2014): 118–20. http://dx.doi.org/10.1016/j.stem.2014.07.010.

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25

Peng, Fenfen, Hongyu Li, Shuting Li, et al. "Correction: Micheliolide ameliorates renal fibrosis by suppressing the Mtdh/BMP/MAPK pathway." Laboratory Investigation 100, no. 5 (2019): 786–87. http://dx.doi.org/10.1038/s41374-019-0301-2.

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26

Chen, Zili, Yifei Ma, Yaozhen Pan, Haitao Zhu, Chao Yu, and Chengyi Sun. "MiR-1297 suppresses pancreatic cancer cell proliferation and metastasis by targeting MTDH." Molecular and Cellular Probes 40 (August 2018): 19–26. http://dx.doi.org/10.1016/j.mcp.2018.06.003.

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27

Kochanek, Dawn M., and David G. Wells. "CPEB1 Regulates the Expression of MTDH/AEG-1 and Glioblastoma Cell Migration." Molecular Cancer Research 11, no. 2 (2013): 149–60. http://dx.doi.org/10.1158/1541-7786.mcr-12-0498.

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28

Hu, Guohong, Yong Wei, and Yibin Kang. "The Multifaceted Role of MTDH/AEG-1 in Cancer Progression: Fig. 1." Clinical Cancer Research 15, no. 18 (2009): 5615–20. http://dx.doi.org/10.1158/1078-0432.ccr-09-0049.

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29

Yuan, Cunzhong, Xiao Li, Shi Yan, Qifeng Yang, Xiaoyan Liu, and Beihua Kong. "The MTDH (−470G>A) Polymorphism Is Associated with Ovarian Cancer Susceptibility." PLoS ONE 7, no. 12 (2012): e51561. http://dx.doi.org/10.1371/journal.pone.0051561.

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30

Guo, Feng, Liling Wan, Aiping Zheng, et al. "Structural Insights into the Tumor-Promoting Function of the MTDH-SND1 Complex." Cell Reports 8, no. 6 (2014): 1704–13. http://dx.doi.org/10.1016/j.celrep.2014.08.033.

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31

El-Ashmawy, Nahla E., Enas A. El-Zamarany, Eman G. Khedr та Mariam A. Abo-Saif. "Activation of EMT in colorectal cancer by MTDH/NF-κB p65 pathway". Molecular and Cellular Biochemistry 457, № 1-2 (2019): 83–91. http://dx.doi.org/10.1007/s11010-019-03514-x.

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32

Fisher, Laura. "Retraction: Long non-coding RNA PCAT1 facilitates cell growth in multiple myeloma through an MTDH-mediated AKT/β-catenin signaling pathway by sponging miR-363-3p". RSC Advances 11, № 11 (2021): 6246. http://dx.doi.org/10.1039/d1ra90071d.

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Retraction of ‘Long non-coding RNA PCAT1 facilitates cell growth in multiple myeloma through an MTDH-mediated AKT/β-catenin signaling pathway by sponging miR-363-3p’ by Ying Chen et al., RSC Adv., 2019, 9, 33834–33842, DOI: 10.1039/C9RA06188F.

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33

Vermeulen, Marijn A., Shusma C. Doebar, Carolien H. M. van Deurzen, John W. M. Martens, Paul J. van Diest, and Cathy B. Moelans. "Copy number profiling of oncogenes in ductal carcinoma in situ of the male breast." Endocrine-Related Cancer 25, no. 3 (2018): 173–84. http://dx.doi.org/10.1530/erc-17-0338.

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Characterizing male breast cancer (BC) and unraveling male breast carcinogenesis is challenging because of the rarity of this disease. We investigated copy number status of 22 BC-related genes in 18 cases of pure ductal carcinoma in situ (DCIS) and in 49 cases of invasive carcinoma (IC) with adjacent DCIS (DCIS-AIC) in males using multiplex ligation-dependent probe amplification (MLPA). Results were compared to female BC and correlated with survival. Overall, copy number ratio and aberration frequency including all 22 genes showed no significant difference between the 3 groups. Individual unpa

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34

Koko, Marwa Y. F., Rokayya Sami, Bertrand Muhoza, Ebtihal Khojah, and Ahmed M. A. Mansour. "Promising Pathway of Thermostable Mannitol Dehydrogenase (MtDH) from Caldicellulosiruptor hydrothermalis 108 for D-Mannitol Synthesis." Separations 8, no. 6 (2021): 76. http://dx.doi.org/10.3390/separations8060076.

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In this study, we conducted the characterization and purification of the thermostable mannitol dehydrogenase (MtDH) from Caldicellulosiruptor hydrothermalis 108. Furthermore, a coupling-enzyme system was designed using (MtDH) from Caldicellulosiruptor hydrothermalis 108 and formate dehydrogenase (FDH) from Ogataea parapolymorpha. The biotransformation system was constructed using Escherichia coli whole cells. The purified enzyme native and subunit molecular masses were 76.7 and 38 kDa, respectively, demonstrating that the enzyme was a dimer. The purified and couple enzyme system results were a

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35

Gu, Chunyan, Lang Feng, Hailin Peng, Hongbao Yang, Zhenqing Feng, and Ye Yang. "MTDH is an oncogene in multiple myeloma, which is suppressed by Bortezomib treatment." Oncotarget 7, no. 4 (2015): 4559–69. http://dx.doi.org/10.18632/oncotarget.6610.

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36

Liu, Dong-Cai, and Zhu-Lin Yang. "MTDH and EphA7 are markers for metastasis and poor prognosis of gallbladder adenocarcinoma." Diagnostic Cytopathology 41, no. 3 (2011): 199–205. http://dx.doi.org/10.1002/dc.21821.

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37

Song, Zhenchuan, Yong Wang, Chao Li, Donghong Zhang, and Xinle Wang. "Molecular Modification of Metadherin/MTDH Impacts the Sensitivity of Breast Cancer to Doxorubicin." PLOS ONE 10, no. 5 (2015): e0127599. http://dx.doi.org/10.1371/journal.pone.0127599.

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38

Salem, Sohair M., Ahmed R. Hamed, and Rehab M. Mosaad. "MTDH and MAP3K1 are direct targets of apoptosis-regulating miRNAs in colorectal carcinoma." Biomedicine & Pharmacotherapy 94 (October 2017): 767–73. http://dx.doi.org/10.1016/j.biopha.2017.07.153.

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39

Cao, Heng, Zhaozhe Liu, Dongchu Ma, Zhenyu Ding, Cheng Du, and Xiaodong Xie. "Downregulation of MTDH using short hairpin RNA inhibited EMT in breast cancer cells." Chinese-German Journal of Clinical Oncology 12, no. 7 (2013): 326–31. http://dx.doi.org/10.1007/s10330-013-1185-z.

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40

Wu, Peng, Dongmei Ye, Jiaoyan Li, et al. "circALPL Sponges miR-127 to Promote Gastric Cancer Progression by Enhancing MTDH Expression." Journal of Cancer 12, no. 16 (2021): 4924–32. http://dx.doi.org/10.7150/jca.49942.

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41

Darbon, J.-M. "MTDH, un gène impliqué à la fois dans le processus métastatique et la chimiorésistance." Bulletin du Cancer 96, no. 3 (2009): 259. http://dx.doi.org/10.1684/bdc.2009.0831.

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42

Wang, Lu, Zhaozhe Liu, Dongchu Ma, et al. "SU6668 suppresses proliferation of triple negative breast cancer cells through down-regulating MTDH expression." Cancer Cell International 13, no. 1 (2013): 88. http://dx.doi.org/10.1186/1475-2867-13-88.

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43

Nikpour, Mahnaz, Modjtaba Emadi-Baygi, Ute Fischer, Günter Niegisch, Wolfgang A. Schulz, and Parvaneh Nikpour. "MTDH/AEG-1 contributes to central features of the neoplastic phenotype in bladder cancer." Urologic Oncology: Seminars and Original Investigations 32, no. 5 (2014): 670–77. http://dx.doi.org/10.1016/j.urolonc.2013.11.005.

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44

He, Juan, Yanan Cao, Tingwei Su, et al. "Downregulation of miR-375 in aldosterone-producing adenomas promotes tumour cell growth via MTDH." Clinical Endocrinology 83, no. 4 (2015): 581–89. http://dx.doi.org/10.1111/cen.12814.

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45

Sassoon, Judyth, Stefan Hörer, Johan Stoop, Hans Mooibroek, and Ulrich Baumann. "Crystallization and preliminary crystallographic analysis of mannitol dehydrogenase (MtDH) from the common mushroomAgaricus bisporus." Acta Crystallographica Section D Biological Crystallography 57, no. 5 (2001): 711–13. http://dx.doi.org/10.1107/s0907444901002542.

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46

Tian, Wuguo, Shuai Hao, Bo Gao, et al. "Lobaplatin inhibits breast cancer progression, cell proliferation while induces cell apoptosis by downregulating MTDH expression." Drug Design, Development and Therapy Volume 12 (October 2018): 3563–71. http://dx.doi.org/10.2147/dddt.s163157.

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47

Liang, Yajun, Jing Hu, Jiatao Li, et al. "Epigenetic Activation of TWIST1 by MTDH Promotes Cancer Stem–like Cell Traits in Breast Cancer." Cancer Research 75, no. 17 (2015): 3672–80. http://dx.doi.org/10.1158/0008-5472.can-15-0930.

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48

Zhang, Mao, Min Li, Na Li, et al. "miR-217 suppresses proliferation, migration, and invasion promoting apoptosis via targeting MTDH in hepatocellular carcinoma." Oncology Reports 37, no. 3 (2017): 1772–78. http://dx.doi.org/10.3892/or.2017.5401.

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49

Qiao, Wenhui, Nong Cao, and Lei Yang. "MicroRNA-154 inhibits the growth and metastasis of gastric cancer cells by directly targeting MTDH." Oncology Letters 14, no. 3 (2017): 3268–74. http://dx.doi.org/10.3892/ol.2017.6558.

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50

Hu, Guohong, Robert A. Chong, Qifeng Yang, et al. "MTDH Activation by 8q22 Genomic Gain Promotes Chemoresistance and Metastasis of Poor-Prognosis Breast Cancer." Cancer Cell 15, no. 1 (2009): 9–20. http://dx.doi.org/10.1016/j.ccr.2008.11.013.

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