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Artykuły w czasopismach na temat „NT2/D1 cells”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Mojsin, Marija, Vladanka Topalovic, Jelena Marjanovic, and Milena Stevanovic. "Quercetin and lithium chloride modulate Wnt signaling in pluripotent embryonal carcinoma NT2/D1 cells." Archives of Biological Sciences 65, no. 1 (2013): 201–9. http://dx.doi.org/10.2298/abs1301201m.

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Wnt signaling functions in numerous cellular activities such as cell fate determination, patterning, and migration in embryogenesis, apoptosis, etc. In this study, we used quercetin and lithium chloride to investigate modulations of the Wnt signaling pathway in human pluripotent embryonal carcinoma NT2/D1 cell line. First, we optimized conditions for NT2/D1 cell treatments with quercetin and lithium chloride and assessed their cytotoxic effects on the cells, cell viability and proliferation rate. Our results showed that induction of cell death by quercetin and LiCl is p53-dependent in NT2/D ce

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Bani-Yaghoub, Mahmud, Josh M. Felker, Mark A. Ozog, John F. Bechberger, and Christian C. G. Naus. "Array analysis of the genes regulated during neuronal differentiation of human embryonal cells." Biochemistry and Cell Biology 79, no. 4 (2001): 387–98. http://dx.doi.org/10.1139/o01-024.

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Recent advances in genetic technology have provided a new platform on which the simultaneous analysis of a large number of genes is possible in a rapid and efficient fashion. To assess the differential expression of human genes during neuronal differentiation, we compared the transcript profiles of undifferentiated, partially differentiated, and fully differentiated NT2/D1 cultures with cDNA expression arrays. Approximately 75 genes (13% of the gene array pool) were differentially expressed during neuronal development of NT2/D1 cells. Genes coding for pyruvate kinase M2 isozyme, clathrin assem

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Sandhu, Jagdeep K., Maria Ribecco-Lutkiewicz, and Abedelnasser Abulrob. "Molecular and Functional Characterization of Caveolae in Mixed Cultures of Human NT-2 Neurons and Astrocytes." Neuroglia 2, no. 1 (2021): 68–88. http://dx.doi.org/10.3390/neuroglia2010008.

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Caveolae are plasma membrane invaginations that are enriched in cholesterol-binding proteins called caveolins. The presence of caveolae and caveolins in mixed cultures of human neurons and glia has not been investigated. Here, we sought to determine the presence of caveolae and caveolins in human NTera-2 (NT2/D1) cells, differentiated with retinoic acid into neuron-like (NT2/N) and astrocyte-like (NT2/A) cells. We found that while caveolin-3 mRNA levels remained relatively constant, caveolin-1 and -2 levels were upregulated in NT2/A and downregulated in NT2/N. No caveolin-1 immunoreactivity wa

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4

DRAKULIC, DANIJELA, JELENA MARJANOVIC VICENTIC, MARIJA SCHWIRTLICH, et al. "The overexpression of SOX2 affects the migration of human teratocarcinoma cell line NT2/D1." Anais da Academia Brasileira de Ciências 87, no. 1 (2015): 389–404. http://dx.doi.org/10.1590/0001-3765201520140352.

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The altered expression of the SOX2 transcription factor is associated with oncogenic or tumor suppressor functions in human cancers. This factor regulates the migration and invasion of different cancer cells. In this study we investigated the effect of constitutive SOX2 overexpression on the migration and adhesion capacity of embryonal teratocarcinoma NT2/D1 cells derived from a metastasis of a human testicular germ cell tumor. We detected that increased SOX2 expression changed the speed, mode and path of cell migration, but not the adhesion ability of NT2/D1 cells. Additionally, we demonstrat

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5

Bani-Yaghoub, Mahmud, Josh M. Felker, and Christian C. G. Naus. "Human NT2/D1 cells differentiate into functional astrocytes." NeuroReport 10, no. 18 (1999): 3843–46. http://dx.doi.org/10.1097/00001756-199912160-00022.

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Eudenbach, Matthias, Jonas Busam, Caroline Bouchard, Oliver Rossbach, Kathi Zarnack, and Uta-Maria Bauer. "Assessment of PRMT6-dependent alternative splicing in pluripotent and differentiating NT2/D1 cells." Life Science Alliance 8, no. 4 (2025): e202402946. https://doi.org/10.26508/lsa.202402946.

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Protein arginine methyltransferase 6 (PRMT6) is a well-characterized epigenetic regulator that methylates histone H3 at arginine 2 (H3R2me2a) in both promoter and enhancer regions, thereby modulating transcriptional initiation. We report here that PRMT6 also regulates gene expression at the post-transcriptional level in the neural pluripotent state and during neuronal differentiation of NT2/D1 cells. PRMT6 knockout causes widespread alternative splicing changes in NT2/D1 cells, most frequently cassette exon alterations. Most of the PRMT6-dependent splicing targets are not transcriptionally aff

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7

Ulisse, Salvatore, Yannick Arlot-Bonnemains, Enke Baldini, et al. "Inhibition of the aurora kinases suppresses in vitro NT2-D1 cell growth and tumorigenicity." Journal of Endocrinology 204, no. 2 (2009): 135–42. http://dx.doi.org/10.1677/joe-09-0257.

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The aurora kinase family members, Aurora-A, -B, and -C (listed as AURKA, AURKB and AURKC respectively in the HUGO Database), are serine/threonine kinases involved in the regulation of chromosome segregation and cytokinesis, and alterations in their expression are associated with malignant cell transformation and genomic instability. Deregulation of the expression of the aurora kinases has been shown to occur also in testicular germ cell tumors (TGCTs) identifying them as putative anticancer therapeutic targets. We here evaluated the in vitro effects of MK-0457, an aurora kinases inhibitor, on

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8

Kovacevic-Grujicic, Natasa, Kazunari Yokoyama, and Milena Stevanovic. "Trans-activation of the human SOX3 promoter by MAZ in NT2/D1 cells." Archives of Biological Sciences 60, no. 3 (2008): 379–87. http://dx.doi.org/10.2298/abs0803379k.

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In this study, we examine the role of three highly conserved putative binding sites for Myc-associated zinc finger protein (MAZ) in regulation of the human SOX3 gene expression. Electrophoretic mobility shift and supershift assays indicate that complexes formed at two out of three MAZ sites of the human SOX3 promoter involve ubiquitously expressed MAZ protein. Furthermore, in cotransfection experiments we demonstrate that MAZ acts as a positive regulator of SOX3 gene transcription in both undifferentiated and RA-differentiated NT2/D1 cells. Although MAZ increased both basal and RA-induced prom

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9

Kanda, Yoshikazu, Kenichiro Katsura, and Sanae Hisayasu. "Milk growth factor (MGF)-induced differentiation of NT2/D1 cells." Neuroscience Letters 384, no. 3 (2005): 260–64. http://dx.doi.org/10.1016/j.neulet.2005.04.098.

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Mojsin, Marija, and Milena Stevanovic. "PBX1 and MEIS1 up-regulate SOX3 gene expression by direct interaction with a consensus binding site within the basal promoter region." Biochemical Journal 425, no. 1 (2009): 107–16. http://dx.doi.org/10.1042/bj20090694.

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Sox3/SOX3 [SRY (sex determining region Y)-box 3] is considered to be one of the earliest neural markers in vertebrates, playing a role in specifying neuronal fate. We have previously reported characterization of the SOX3 promoter and demonstrated that the general transcription factors NF-Y (nuclear factor-Y), Sp1 (specificity protein 1) and USF (upstream stimulatory factor) are involved in transcriptional regulation of SOX3 promoter activity. In the present study we provide the first evidence that the TALE (three-amino-acid loop extension) transcription factors PBX1 (pre-B-cell leukaemia homeo

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11

Klajn, A., D. Drakulic, M. Tosic, Z. Pavkovic, M. Schwirtlich, and M. Stevanovic. "SOX2 overexpression affects neural differentiation of human pluripotent NT2/D1 cells." Biochemistry (Moscow) 79, no. 11 (2014): 1172–82. http://dx.doi.org/10.1134/s0006297914110042.

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12

Jezierski, Anna, Paromita Deb-Rinker, Caroline Sodja, et al. "Involvement ofNOS3in RA-Induced neural differentiation of human NT2/D1 cells." Journal of Neuroscience Research 90, no. 12 (2012): 2362–77. http://dx.doi.org/10.1002/jnr.23118.

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13

Chu, Wing-Keung, Li-Man Hung, Chun-Wei Hou, and Jan-Kan Chen. "MicroRNA 630 Represses NANOG Expression through Transcriptional and Post-Transcriptional Regulation in Human Embryonal Carcinoma Cells." International Journal of Molecular Sciences 23, no. 1 (2021): 46. http://dx.doi.org/10.3390/ijms23010046.

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The pluripotent transcription factor NANOG is essential for maintaining embryonic stem cells and driving tumorigenesis. We previously showed that PKC activity is involved in the regulation of NANOG expression. To explore the possible involvement of microRNAs in regulating the expression of key pluripotency factors, we performed a genome-wide analysis of microRNA expression in the embryonal carcinoma cell line NT2/D1 in the presence of the PKC activator, PMA. We found that MIR630 was significantly upregulated in PMA-treated cells. Experimentally, we showed that transfection of MIR630 mimic into

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14

Ludbrook, Louisa, Dimuthu Alankarage, Stefan Bagheri-Fam, and Vincent Harley. "Dataset of differentially expressed genes from SOX9 over-expressing NT2/D1 cells." Data in Brief 9 (December 2016): 194–98. http://dx.doi.org/10.1016/j.dib.2016.08.047.

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15

Yao, Z. X., Z. Han, J. Xu, J. Greeson, L. Lecanu, and V. Papadopoulos. "22R-Hydroxycholesterol induces differentiation of human NT2 precursor (Ntera2/D1 teratocarcinoma) cells." Neuroscience 148, no. 2 (2007): 441–53. http://dx.doi.org/10.1016/j.neuroscience.2007.06.013.

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Abraham, I., K. E. Sampson, E. A. Powers, J. K. Mayo, V. A. Ruff, and K. L. Leach. "Increased PKA and PKC activities accompany neuronal differentiation of NT2/D1 cells." Journal of Neuroscience Research 28, no. 1 (1991): 29–39. http://dx.doi.org/10.1002/jnr.490280104.

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Ivković, Ivana, Miroslav Novaković, Milan Veljić, et al. "Bis-Bibenzyls from the Liverwort Pellia endiviifolia and Their Biological Activity." Plants 10, no. 6 (2021): 1063. http://dx.doi.org/10.3390/plants10061063.

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Based on previous investigations where bis-bibenzyls isolated from liverworts showed various biological activities (cytotoxic, antimicrobial, and antiviral), we investigated their cytotoxic activity in several human cancer cell lines. From the methylene-chloride/methanol extract of the liverwort Pellia endiviifolia, three bis-bibenzyls of the perrottetin type were isolated, namely perrottetin E, 10′-hydroxyperrottetin E, and 10,10′-dihydroxyperrottetin E. The last two were found for the first time in this species. Their structures were resolved using 1D and 2D NMR, as well as by comparison wit

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18

Chan, S., CJ McCabe, TJ Visser, JA Franklyn, and MD Kilby. "Thyroid hormone responsiveness in N-Tera-2 cells." Journal of Endocrinology 178, no. 1 (2003): 159–67. http://dx.doi.org/10.1677/joe.0.1780159.

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N-TERA-2 cl/D1 (NT2) cells, a human embryonal cell line with characteristics of central nervous system precursor cells, were utilised to study thyroid hormone action during early neuronal growth and differentiation. Undifferentiated NT2 cells expressed mRNAs encoding thyroid hormone receptors (TRs) alpha1, alpha2 and beta1, iodothyronine deiodinases types 2 (D2) and 3 (D3) (which act as the pre-receptor regulators), and the thyroid hormone-responsive genes myelin basic protein (MBP) and neuroendocrine specific protein A (NSP-A). When terminally differentiated into post-mitotic neurons (hNT), T

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19

Radhakrishnan, Karthika, Michael Luu, Josie Iaria, et al. "Activin and BMP Signalling in Human Testicular Cancer Cell Lines, and a Role for the Nucleocytoplasmic Transport Protein Importin-5 in Their Crosstalk." Cells 12, no. 7 (2023): 1000. http://dx.doi.org/10.3390/cells12071000.

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Testicular germ cell tumours (TGCTs) are the most common malignancy in young men. Originating from foetal testicular germ cells that fail to differentiate correctly, TGCTs appear after puberty as germ cell neoplasia in situ cells that transform through unknown mechanisms into distinct seminoma and non-seminoma tumour types. A balance between activin and BMP signalling may influence TGCT emergence and progression, and we investigated this using human cell line models of seminoma (TCam-2) and non-seminoma (NT2/D1). Activin A- and BMP4-regulated transcripts measured at 6 h post-treatment by RNA-s

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Shyu, Rong-Yaun, Chun-Hua Wang, Chang-Chieh Wu, et al. "Tazarotene-Induced Gene 1 (TIG1) Interacts with Serine Protease Inhibitor Kazal-Type 2 (SPINK2) to Inhibit Cellular Invasion of Testicular Carcinoma Cells." BioMed Research International 2019 (November 25, 2019): 1–10. http://dx.doi.org/10.1155/2019/6171065.

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Tazarotene-induced gene 1 (TIG1) encodes a protein that is a retinoid-regulated tumor suppressor. TIG1 is expressed in most normal tissues, and downregulation of TIG1 expression in multiple cancers is caused by promoter hypermethylation. Kazal-type serine protease inhibitor-2 (SPINK2) is a serine protease inhibitor, and the SPINK protein family has been shown to inhibit the expression of urokinase-type plasminogen activator (uPA). In addition, increased levels of uPA and the uPA receptor were observed in testicular cancer tissues. This study demonstrated that TIG1 interacts with SPINK2 in NT2/

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21

Radonjic, Mia, Jelena Petrovic, Milena Milivojevic, Milena Stevanovic, Jasmina Stojkovska, and Bojana Obradovic. "Chemical engineering methods in analyses of 3D cancer cell cultures: Hydrodinamic and mass transport considerations." Chemical Industry and Chemical Engineering Quarterly, no. 00 (2021): 33. http://dx.doi.org/10.2298/ciceq210607033r.

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A multidisciplinary approach based on experiments and mathematical modeling was used in biomimetic system development for three-dimensional (3D) cultures of cancer cells. Specifically, two cancer cell lines, human embryonic teratocarcinoma NT2/D1 and rat glioma C6, were immobilized in alginate microbeads and microfibers, respectively, and cultured under static and flow conditions in perfusion bioreactors, while chemical engineering methods were applied to explain the obtained results. The superficial medium velocity of 80 mm s-1 induced lower viability of NT2/D1 cells in superficial microbead

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22

Mojsin, Marija, Vladanka Topalovic, Jelena Marjanovic Vicentic та ін. "Crosstalk between SOXB1 proteins and WNT/β-catenin signaling in NT2/D1 cells". Histochemistry and Cell Biology 144, № 5 (2015): 429–41. http://dx.doi.org/10.1007/s00418-015-1352-0.

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Balint, Vanda, Mina Peric, Sanja Dacic, et al. "The Role of SOX2 and SOX9 Transcription Factors in the Reactivation-Related Functional Properties of NT2/D1-Derived Astrocytes." Biomedicines 12, no. 4 (2024): 796. http://dx.doi.org/10.3390/biomedicines12040796.

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Astrocytes are the main homeostatic cells in the central nervous system, with the unique ability to transform from quiescent into a reactive state in response to pathological conditions by reacquiring some precursor properties. This process is known as reactive astrogliosis, a compensatory response that mediates tissue damage and recovery. Although it is well known that SOX transcription factors drive the expression of phenotype-specific genetic programs during neurodevelopment, their roles in mature astrocytes have not been studied extensively. We focused on the transcription factors SOX2 and

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Savic, Tijana, Milena Stevanovic, and Gordana Nikcevic. "Retinoic acid-induced SoX3 gene expression in NT2/D1 cells is RXR homodimer-independent." Archives of Biological Sciences 61, no. 4 (2009): 631–38. http://dx.doi.org/10.2298/abs0904631s.

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The Sox3/SOX3 gene is implicated in the control of nervous system development. We previously demon?strated modulation of human SOX3 gene expression during neural induction of NT2/D1 cells by retinoic acid (RA). Also, we accurately verified RXR retinoid receptors as major mediators of the effect of RA on SOX3 expression, and excluded RARs as its heterodimeric partners in RA-SOX3 signaling. Here we present evidence that activation of the SOX3 gene by RA is not RXR homodimer-dependent. The described line of SOX3 gene expression studies is valuable for future investigation of the impact that this

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Wang, Shu, Lars E. Rosengren, Anders Hamberger, and Kenneth G. Haglid. "An acquired sensitivity to H2O2-induced apoptosis during neuronal differentiation of NT2/D1 cells." NeuroReport 9, no. 14 (1998): 3207–11. http://dx.doi.org/10.1097/00001756-199810050-00014.

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Tarczyluk, Marta A., David A. Nagel, John D. O’Neil, et al. "Functional Astrocyte-Neuron Lactate Shuttle in a Human Stem Cell-Derived Neuronal Network." Journal of Cerebral Blood Flow & Metabolism 33, no. 9 (2013): 1386–93. http://dx.doi.org/10.1038/jcbfm.2013.81.

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The NT2.D1 cell line is one of the most well-documented embryocarcinoma cell lines, and can be differentiated into neurons and astrocytes. Great focus has also been placed on defining the electrophysiological properties of the neuronal cells, and more recently we have investigated the functional properties of their associated astrocytes. We now show for the first time that human stem cell-derived astrocytes produce glycogen and that co-cultures of these cells demonstrate a functional astrocyte-neuron lactate shuttle (ANLS). The ANLS hypothesis proposes that during neuronal activity, glutamate

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Onganía, Gabriela Naum, and Rolando Rivera Pomar. "Non-Muscle Myosin IIA (Myh9) is in the Nucleus of S-Phase Entering NT2-D1 Cells." Journal of Nutritional Therapeutics 7, no. 2 (2018): 59–66. http://dx.doi.org/10.6000/1929-5634.2018.07.02.4.

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Tsai, Yung-Chieh, Yen-Ni Teng, Jui-Hsiang Hung, et al. "Correlation between leucine rich domain and the stability of LRWD1 protein in human NT2/D1 cells." Advances in Medical Sciences 59, no. 2 (2014): 266–72. http://dx.doi.org/10.1016/j.advms.2014.07.002.

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Yan, Hong-Tao, Toshikatsu Shinka, Youichi Sato, et al. "Overexpression of SOX15 Inhibits Proliferation of NT2/D1 Cells Derived from a Testicular Embryonal Cell Carcinoma." Molecules and Cells 24, no. 3 (2007): 323–28. http://dx.doi.org/10.1016/s1016-8478(23)07346-6.

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Drakulic, Danijela, Milena Stevanovic, and Gordana Nikcevic. "Gene expression analysis by non-radioactive RNA-RNA in situ hybridization techniques." Jugoslovenska medicinska biohemija 23, no. 2 (2004): 127–33. http://dx.doi.org/10.2298/jmh0402127d.

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RNA-RNA in situ hybridization is a reliable method for studying tissue and cell specific gene expression, which enables visualization of labeled antisense RNA probe hybridized to specific mRNA. In this study we employed non-radioactive RNA-RNA in situ hybridization using biotin- or digoxigenin-labeled RNA probes in order to detect SOX gene expression in carcinoma cell lines. By this approach we confirmed results obtained by Northern blot analysis, where the presence of SOX2 mRNA in NT2/D1 and SOX14 mRNA in HepG2 cells has been established. Our aim was to set up RNA-RNA in situ hybridization me

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Milivojevic, Milena, Gordana Nikcevic, Natasa Kovacevic-Grujicic та ін. "Involvement of ubiquitous and tale transcription factors, as well as liganded RXRα, in the regulation of human SOX2 gene expression in the NT2/D1 embryonal carcinoma cell line". Archives of Biological Sciences 62, № 2 (2010): 199–210. http://dx.doi.org/10.2298/abs1002199m.

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SOX2 is a key transcription factor in embryonic development representing a universal marker of pluripotent stem cells. Based on the functional redundancy and overlapping expression patterns of SOXB1 subgroup members during development, the goal of this study has been to analyze if some aspects of regulation of expression are preserved between human SOX2 and SOX3 genes. Thus, we have tested several transcription factors previously demonstrated to play roles in controlling SOX3 gene activity for potential participation in the regulation of SOX2 gene expression in NT2/D1 cells. Here we report on

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Topalovic, Vladanka, Aleksandar Krstic, Marija Schwirtlich, et al. "Epigenetic regulation of human SOX3 gene expression during early phases of neural differentiation of NT2/D1 cells." PLOS ONE 12, no. 9 (2017): e0184099. http://dx.doi.org/10.1371/journal.pone.0184099.

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Xu, M., G. N. Zhao, X. Lv, et al. "CTCF Controls HOXA Cluster Silencing and Mediates PRC2-Repressive Higher-Order Chromatin Structure in NT2/D1 Cells." Molecular and Cellular Biology 34, no. 20 (2014): 3867–79. http://dx.doi.org/10.1128/mcb.00567-14.

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Wan, Carthur K., Simon J. O'Carroll, Sue-Ling Kim, Colin R. Green, and Louise F. B. Nicholson. "Spatiotemporal changes in Cx30 and Cx43 expression during neuronal differentiation of P19 EC and NT2/D1 cells." Cell Biology International Reports 20, no. 2 (2013): 13–23. http://dx.doi.org/10.1002/cbi3.10005.

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Macheroni, Carla, Thaís Fabiana Gameiro Lucas, Deborah Simão Souza, et al. "Activation of estrogen receptor ESR1 and ESR2 induces proliferation of the human testicular embryonal carcinoma NT2/D1 cells." Molecular and Cellular Endocrinology 554 (August 2022): 111708. http://dx.doi.org/10.1016/j.mce.2022.111708.

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Macheroni, Carla, Deborah Simão Souza, Catarina Segreti Porto, and Carolina Meloni Vicente. "Estrogen receptor activates SRC and ERK1/2 and promotes tumorigenesis in human testicular embryonic carcinoma cells NT2/D1." Experimental Cell Research 442, no. 2 (2024): 114282. http://dx.doi.org/10.1016/j.yexcr.2024.114282.

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Katschnig, Matthias, Boris Maroh, Natascha Andraschek, et al. "Cell Morphology on Poly(methyl methacrylate) Microstructures as Function of Surface Energy." International Journal of Biomaterials 2019 (May 2, 2019): 1–12. http://dx.doi.org/10.1155/2019/2393481.

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Whilst the significance of substrate topography as a regulator of cell function is well established, a systematic analysis of the principles underlying this is still unavailable. Here we evaluate the hypothesis that surface energy plays a decisive role in substrate-mediated modulation of cell phenotype by evaluation of cell behaviour on synthetic microstructures exhibiting pronounced differences in surface energy. These microstructures, specifically cubes and walls, were fabricated from a biocompatible base polymer, poly(methyl methacrylate), by variotherm injection molding. The dimensions of

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Chadalavada, Rajendrakumar S. V., James E. Korkola, Jane Houldsworth, et al. "Constitutive Gene Expression Predisposes Morphogen-Mediated Cell Fate Responses of NT2/D1 and 27X-1 Human Embryonal Carcinoma Cells." STEM CELLS 25, no. 3 (2006): 771–78. http://dx.doi.org/10.1634/stemcells.2006-0271.

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Ferreira, Stéphanie, Marie-Joëlle Dupire, André Delacourte, Jamila Najib, and Marie-Laure Caillet-Boudin. "Synthesis and Regulation of Apolipoprotein E during the Differentiation of Human Neuronal Precursor NT2/D1 Cells into Postmitotic Neurons." Experimental Neurology 166, no. 2 (2000): 415–21. http://dx.doi.org/10.1006/exnr.2000.7510.

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Díaz, Víctor M., Silvia Mori, Elena Longobardi, et al. "p160 Myb-Binding Protein Interacts with Prep1 and Inhibits Its Transcriptional Activity." Molecular and Cellular Biology 27, no. 22 (2007): 7981–90. http://dx.doi.org/10.1128/mcb.01290-07.

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ABSTRACT Prep1 is known to interact in vivo with Pbx1 to regulate development and organogenesis. We have identified a novel Prep1-interacting protein, p160 c-Myb binding protein (p160). p160 and Pbx1 compete for Prep1 in vitro, and p160 inhibits Prep1-dependent HoxB2 expression in retinoic acid-treated NT2-D1 cells. The N-terminal physiologically truncated form of p160, p67, binds the sequence 63LFPLL67 in the HR1 domain of Prep1. Mutation of both L63 and L66 impairs the binding of Prep1 to both p160/p67 and Pbx1. The sequences required to bind Prep1 are mainly located in residues 51 to 151. I

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Lei, W., T. Hirose, L.-X. Zhang, et al. "Cloning of the human orphan receptor germ cell nuclear factor/retinoid receptor-related testis-associated receptor and its differential regulation during embryonal carcinoma cell differentiation." Journal of Molecular Endocrinology 18, no. 2 (1997): 167–76. http://dx.doi.org/10.1677/jme.0.0180167.

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ABSTRACT We have cloned a cDNA encoding the full-length coding region of the human homologue of the germ cell nuclear factor (GCNF)/retinoid receptor-related testis-associated receptor (RTR), from a human testis cDNA library. The amino acid sequence of human GCNF/RTR is highly homologous to that of the mouse GCNF/RTR. The largest difference between the two homologues is a 15 amino acid deletion in the human GCNF/RTR at amino acid 47. The GCNF/RTR gene was localized on human chromosome 9. Northern blot analysis using poly(A)+ RNA from different human tissues showed that GCNF/RTR mRNA is most ab

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Kovacevic-Grujicic, Natasa, Marija Mojsin, Jelena Popovic, Isidora Petrovic, Vladanka Topalovic, and Milena Stevanovic. "Cyclic AMP response element binding (CREB) protein acts as a positive regulator of SOX3 gene expression in NT2/D1 cells." BMB Reports 47, no. 4 (2014): 197–202. http://dx.doi.org/10.5483/bmbrep.2014.47.4.084.

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Topalovic, V., M. Schwirtlich, M. Stevanovic, and M. Mojsin. "Histone modifications on the promoters of human OCT4 and NANOG genes at the onset of neural differentiation of NT2/D1 cells." Biochemistry (Moscow) 82, no. 6 (2017): 715–22. http://dx.doi.org/10.1134/s0006297917060086.

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BYRD, ANGÈLE S., MARIANNA SIKORSKA, P. ROY WALKER, and JAGDEEP K. SANDHU. "Effects of glutathione depletion on the viability of human NT2-derived neuronal and astroglial cultures." Neuron Glia Biology 1, no. 4 (2004): 317–26. http://dx.doi.org/10.1017/s1740925x05000207.

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The level of glutathione (GSH) is often reduced in brains that are affected by neurodegeneration. It is not known, however, whether this is a cause or a consequence of the disease. Here we have examined the effects of GSH depletion on the viability of human neurons cultured in either the presence or the absence of astrocytes, both derived from NT2/D1 cells. We established that the endogenous concentration of GSH is 10 times lower in neurons than in astrocytes (1.42 versus 18.9 pmol µg protein−1) and that pure neuronal cultures begin to die by apoptosis within 24 h of GSH depletion. By contrast

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Mao, Pingping, Mary P. Hever, Lynne M. Niemaszyk, et al. "Serine/Threonine Kinase 17A Is a Novel p53 Target Gene and Modulator of Cisplatin Toxicity and Reactive Oxygen Species in Testicular Cancer Cells." Journal of Biological Chemistry 286, no. 22 (2011): 19381–91. http://dx.doi.org/10.1074/jbc.m111.218040.

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Testicular cancer is highly curable with cisplatin-based therapy, and testicular cancer-derived human embryonal carcinoma (EC) cells undergo a p53-dominant transcriptional response to cisplatin. In this study, we have discovered that a poorly characterized member of the death-associated protein family of serine/threonine kinases, STK17A (also called DRAK1), is a novel p53 target gene. Cisplatin-mediated induction of STK17A in the EC cell line NT2/D1 was prevented with p53 siRNA. Furthermore, STK17A was induced with cisplatin in HCT116 and MCF10A cells but to a much lesser extent in isogenic p5

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Stevanović, Milena, Danijela Drakulić, Marija Švirtlih, et al. "SOX2 gene – master regulator of numerous cellular processes." Biologia Serbica 39, no. 1 (2017): 9–15. https://doi.org/10.5281/zenodo.826595.

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<strong>S</strong><strong>ummary.</strong> The SOX (Sry-related HMG box) proteins comprise a group of transcription factors that act as key regulators of diverse developmental and physiological processes, ranging from blastocyst and germ layer formation to differentiation into adult tissues and organs. SOX proteins influence survival and proliferation, as well as cell fate decisions and consecutive lineage progression. Accordingly, SOX proteins are involved in multiple events, from maintenance of stem cells pluripotency, to driving their terminal differentiation into specialized cell types. Th

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Pierce, Tanya, Howard J. Worman, and Jon Holy. "Neuronal Differentiation of NT2/D1 Teratocarcinoma Cells Is Accompanied by a Loss of Lamin A/C Expression and an Increase in Lamin B1 Expression." Experimental Neurology 157, no. 2 (1999): 241–50. http://dx.doi.org/10.1006/exnr.1999.7060.

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Macheroni, Carla, Giuseppe Gianini Figueirêdo Leite, Deborah Simão Souza, et al. "Activation of estrogen receptor induces differential proteomic responses mainly involving migration, invasion, and tumor development pathways in human testicular embryonal carcinoma NT2/D1 cells." Journal of Steroid Biochemistry and Molecular Biology 237 (March 2024): 106443. http://dx.doi.org/10.1016/j.jsbmb.2023.106443.

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Curatola, A. M., and C. Basilico. "Expression of the K-fgf proto-oncogene is controlled by 3' regulatory elements which are specific for embryonal carcinoma cells." Molecular and Cellular Biology 10, no. 6 (1990): 2475–84. http://dx.doi.org/10.1128/mcb.10.6.2475-2484.1990.

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Expression of the K-fgf/hst proto-oncogene appears to be restricted to cells in the early stages of development, such as embryonal carcinoma (EC) cells. When EC cells are induced to differentiate, K-fgf expression is drastically repressed. To identify cis-acting DNA elements responsible for this type of regulation, we constructed a plasmid in which cat gene expression was driven by about 1 kilobase of upstream K-fgf human DNA sequences, including the putative promoter, and transfected it into undifferentiated F9 EC cells or HeLa cells as prototypes of cells which express or do not express, res

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Curatola, A. M., and C. Basilico. "Expression of the K-fgf proto-oncogene is controlled by 3' regulatory elements which are specific for embryonal carcinoma cells." Molecular and Cellular Biology 10, no. 6 (1990): 2475–84. http://dx.doi.org/10.1128/mcb.10.6.2475.

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Expression of the K-fgf/hst proto-oncogene appears to be restricted to cells in the early stages of development, such as embryonal carcinoma (EC) cells. When EC cells are induced to differentiate, K-fgf expression is drastically repressed. To identify cis-acting DNA elements responsible for this type of regulation, we constructed a plasmid in which cat gene expression was driven by about 1 kilobase of upstream K-fgf human DNA sequences, including the putative promoter, and transfected it into undifferentiated F9 EC cells or HeLa cells as prototypes of cells which express or do not express, res

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