The DOI matches its Crossref record; 77 of the 77 references it cites were found in a registry or an index.
Molecular and epigenetic pathogenesis of germ cell tumors
Open accessAbstract
The development of germ cell tumors (GCTs) is a unique pathogenesis occurring at an early developmental stage during specification, migration or colonization of primordial germ cells (PGCs) in the genital ridge. Since driver mutations could not be identified so far, the involvement of the epigenetic machinery during the pathogenesis seems to play a crucial role. Currently, it is investigated whether epigenetic modifications occurring between the omnipotent two-cell stage and the pluripotent implanting PGCs might result in disturbances eventually leading to GCTs. Although progress in understanding epigenetic mechanisms during PGC development is ongoing, little is known about the complete picture of its involvement during GCT development and eventual classification into clinical subtypes. This review will shed light into the current knowledge of the complex epigenetic and molecular contribution during pathogenesis of GCTs by emphasizing on early developmental stages until arrival of late PGCs in the gonads. We questioned how misguided migrating and/or colonizing PGCs develop to either type I or type II GCTs. Additionally, we asked how pluripotency can be regulated during PGC development and which epigenetic changes contribute to GCT pathogenesis. We propose that SOX2 and SOX17 determine either embryonic stem cell-like (embryonal carcinoma) or PGC-like cell fate (seminoma). Finally, we suggest that factors secreted by the microenvironment, i.e. BMPs and BMP inhibiting molecules, dictate the fate decision of germ cell neoplasia in situ (into seminoma and embryonal carcinoma) and seminomas (into embryonal carcinoma or extraembryonic lineage), indicating an important role of the microenvironment on GCT plasticity.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Figures
![Figure 1 Development of GCs and pathogenesis of TGCTs. Upper panel: Development of the human embryo from the zygote (0 day post fertilization [dpf]) until Week 6 post fertilization when the PGC reach the gonads. Lower panel: DNA methylation events during PGC migration and arrival at the genital ridge and where different types pf TGCTs are thought to originate from. The table summarizes molecular and epigenetic findings from this review. Data from Refs. [1,48,49,52,58,74]. PGC, primordial germ cell; ICM, inner cell mass; SE, seminoma; EC, embryonal carcinoma; CC, choriocarcinoma; TE, teratoma; YST, yolk sac tumor; NS, non-seminoma; GCNIS, germ cell neoplasia in situ; GC, germ cell; TGCTs, testicular germ cell tumors.](/paper-figures/be652bd315284e418846ea65943685f9/molecular-and-epigenetic-pathogenesis-of-germ-cell-tumors-figure-1.jpg)
![Figure 2 Plasticity of SE cells—Transformation into EC and CC/YST. Depending on BMP activity GCNIS either develop into SE (BMP active) or EC (BMP inhibited) which further differentiates into TE, CC and YST. Additionally, to the commonly accepted TGCT developmental theory (Fig. 1), in vitro experiments indicated reprogramming of SE to EC [22] as well as directly into extraembryonal tumors without EC intermediate (SOX2) [44,75]. SE to EC transformation is initiated in vitro by BMP inhibition through the microenvironment. SOX2 upregulation and establishment of NODAL signaling give rise to mixed SE/EC. These can further differentiate into mixed SE/NS, eventually leading to mixed tumors with SE components while also containing extraembryonal proportions. Direct SE differentiation into extraembryonal-like tissue has been demonstrated in vitro and in vivo although the factors involved in the latter still remain unknown and have yet to be determined. GCNIS, germ cell neoplasia in situ; EC, embryonal carcinoma; SE, seminoma; NS, non-seminoma; CC, choriocarcinoma; TE, teratoma; YST, yolk sac tumor; NS, non-seminoma; GC, germ cell; TGCT, testicular germ cell tumor.](/paper-figures/e437b4174fb2445bb274139ec97796d9/molecular-and-epigenetic-pathogenesis-of-germ-cell-tumors-figure-2.jpg)
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In TGCTs, the relationship between malignant cells and the surrounding tumor microenvironment (TME) seems to play an important role in the disruption of this balance [16,17,18,19].”
From The Immune Landscape and Immunotherapeutic Strategies in Platinum-Refractory Testicular Germ Cell Tumors (2024) · cites this paper as [19]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Takahashi, K., & Yamanaka, S. (2006) · Cell · doi:10.1016/j.cell.2006.07.024 · Cited by 26,673
Skakkebæk, N. E., Rajpert-De Meyts, E., & Main, K. M. (2001) · Human Reproduction · doi:10.1093/humrep/16.5.972 · Cited by 2,260
G-protein-coupled receptors and cancer
Dorsam, R. T., & Gutkind, J. S. (2007) · Nature reviews. Cancer · doi:10.1038/nrc2069 · Cited by 1,456
Reconstitution of the Mouse Germ Cell Specification Pathway in Culture by Pluripotent Stem Cells
Hayashi, K., Ohta, H., Kurimoto, K., Aramaki, S., & Saitou, M. (2011) · Cell · doi:10.1016/j.cell.2011.06.052 · Cited by 1,379
N6-methyladenosine modification destabilizes developmental regulators in embryonic stem cells
Wang, Y., Li, Y., Toth, J. I., Petroski, M. D., Zhang, Z., & Zhao, J. C. (2014) · Nature Cell Biology · doi:10.1038/ncb2902 · Cited by 1,290
Schwartz, S., Mumbach, M. R., Jovanovic, M., Wang, T., Maciag, K., Bushkin, G. G., Mertins, P., Ter-Ovanesyan, D., Habib, N., Cacchiarelli, D., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.05.048 · Cited by 1,216
m6A RNA Modification Controls Cell Fate Transition in Mammalian Embryonic Stem Cells
Batista, P. J., Molinie, B., Wang, J., Qu, K., Zhang, J., Li, L., Bouley, D. M., Lujan, E., Haddad, B., Daneshvar, K., et al. (2014) · Cell Stem Cell · doi:10.1016/j.stem.2014.09.019 · Cited by 1,203
Testicular germ-cell tumours in a broader perspective
Oosterhuis, J. W., & Looijenga, L. H. J. (2005) · Nature Reviews Cancer · doi:10.1038/nrc1568 · Cited by 916
Epigenetic events in mammalian germ-cell development: reprogramming and beyond
Sasaki, H., & Matsui, Y. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2295 · Cited by 871
SOX17 Is a Critical Specifier of Human Primordial Germ Cell Fate
Irie, N., Weinberger, L., Tang, W. W. C., Kobayashi, T., Viukov, S. V., Manor, Y. S., Dietmann, S., Hanna, J. H., & Surani, M. A. (2014) · Cell · doi:10.1016/j.cell.2014.12.013 · Cited by 864
Guidance of Primordial Germ Cell Migration by the Chemokine SDF-1
Doitsidou, M., Reichman-Fried, M., Stebler, J., Köprunner, M., Dörries, J., Meyer, D., Esguerra, C. V., Leung, T., & Raz, E. (2002) · Cell · doi:10.1016/s0092-8674(02)01135-2 · Cited by 697
Mechanisms guiding primordial germ cell migration: strategies from different organisms
Richardson, B. E., & Lehmann, R. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2815 · Cited by 505
The chemokine SDF1/CXCL12 and its receptor CXCR4 regulate mouse germ cell migration and survival
Molyneaux, K. A., Zinszner, H., Kunwar, P. S., Schaible, K., Stebler, J., Sunshine, M. J., O'Brien, W., Raz, E., Littman, D., Wylie, C., et al. (2003) · Development · doi:10.1242/dev.00640 · Cited by 469
Kurimoto, K., Yabuta, Y., Ohinata, Y., Shigeta, M., Yamanaka, K., & Saitou, M. (2008) · Genes & Development · doi:10.1101/gad.1649908 · Cited by 352
Ara, T., Nakamura, Y., Egawa, T., Sugiyama, T., Abe, K., Kishimoto, T., Matsui, Y., & Nagasawa, T. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0730719100 · Cited by 346
Human germ cell tumours from a developmental perspective
Oosterhuis, J. W., & Looijenga, L. H. J. (2019) · Nature Reviews Cancer · doi:10.1038/s41568-019-0178-9 · Cited by 328
ERM is required for transcriptional control of the spermatogonial stem cell niche
Chen, C., Ouyang, W., Grigura, V., Zhou, Q., Carnes, K., Lim, H., Zhao, G.-Q., Arber, S., Kurpios, N., Murphy, T. L., et al. (2005) · Nature · doi:10.1038/nature03894 · Cited by 321
Germ cell specification in mice
Saitou, M. (2009) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2009.06.003 · Cited by 298
Germ Cell Specification in Mice
Hayashi, K., de Sousa Lopes, S. M. C., & Surani, M. A. (2007) · Science · doi:10.1126/science.1137545 · Cited by 254
de Jong, J., Stoop, H., Gillis, A., van Gurp, R., van de Geijn, G., de Boer, M., Hersmus, R., Saunders, P. T. K., Anderson, R., Oosterhuis, J. W., et al. (2008) · The Journal of Pathology · doi:10.1002/path.2332 · Cited by 241
Critical Function of AP-2gamma/TCFAP2C in Mouse Embryonic Germ Cell Maintenance1
Weber, S., Eckert, D., Nettersheim, D., Gillis, A., Schäfer, S., Kuckenberg, P., Ehlermann, J., Werling, U., Biermann, K., Looijenga, L. H. J., et al. (2009) · Biology of Reproduction · doi:10.1095/biolreprod.109.078717 · Cited by 217
Self-citationPrimordial germ cell migration in the chick and mouse embryo: the role of the chemokine SDF-1/CXCL12
Stebler, J., Spieler, D., Slanchev, K., Molyneaux, K. A., Richter, U., Cojocaru, V., Tarabykin, V. S., Wylie, C., Kessel, M., & Raz, E. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.05.009 · Cited by 215
Oct4 switches partnering from Sox2 to Sox17 to reinterpret the enhancer code and specify endoderm
Aksoy, I., Jauch, R., Chen, J., Dyla, M., Divakar, U., Bogu, G. K., Teo, R., Ng, C. K. L., Herath, W. B., Li-li, S., et al. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.31 · Cited by 202
Hoei‐Hansen, C. E., Holm, M. L., Meyts, E. R., & Skakkebæk, N. E. (2003) · The Journal of Pathology · doi:10.1002/path.1372 · Cited by 201
Kojima, Y., Sasaki, K., Yokobayashi, S., Sakai, Y., Nakamura, T., Yabuta, Y., Nakaki, F., Nagaoka, S. I., Woltjen, K., Hotta, A., et al. (2017) · Cell stem cell · doi:10.1016/j.stem.2017.09.005 · Cited by 190
Distinct epigenetic phenotypes in seminomatous and nonseminomatous testicular germ cell tumors
Smiraglia, D. J., Szymanska, J., Kraggerud, S. M., Lothe, R. A., Peltomäki, P., & Plass, C. (2002) · Oncogene · doi:10.1038/sj.onc.1205488 · Cited by 172
Berney, D. M., Looijenga, L. H. J., Idrees, M. T., et al. (2016) · Histopathology · doi:10.1111/his.12958 · Cited by 169
Skakkebæk, N. E., Holm, M. L., Hoei‐Hansen, C. E., Jørgensen, N., & Meyts, E. R. (2003) · Apmis · doi:10.1034/j.1600-0463.2003.11101031.x · Cited by 165
Human Germ Cell Tumors are Developmental Cancers: Impact of Epigenetics on Pathobiology and Clinic
Lobo, J., Gillis, A., Jerónimo, C., Henrique, R., & Looijenga, L. H. J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20020258 · Cited by 143
Netto, G. J., Nakai, Y., Nakayama, M., Jadallah, S., Toubaji, A., Nonomura, N., Albadine, R., Hicks, J. L., Epstein, J. I., Yegnasubramanian, S., et al. (2008) · Modern Pathology · doi:10.1038/modpathol.2008.127 · Cited by 125
Eckert, D., Biermann, K., Nettersheim, D., Gillis, A., Steger, K., Jäck, H., Müller, A. M., Looijenga, L. H. J., & Schorle, H. (2008) · BMC Developmental Biology · doi:10.1186/1471-213x-8-106 · Cited by 122
Self-citationMammalian germ cells are determined after PGC colonization of the nascent gonad
Nicholls, P. K., Schorle, H., Naqvi, S., Hu, Y., Fan, Y., Carmell, M. A., Dobrinski, I., Watson, A. L., Carlson, D. F., Fahrenkrug, S. C., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1910733116 · Cited by 122
Endogenous Nodal signaling regulates germ cell potency during mammalian testis development
Spiller, C. M., Feng, C.-W. A., Jackson, A., Gillis, A., Rolland, A. D., Looijenga, L. H. J., Koopman, P. A., & Bowles, J. (2012) · Development · doi:10.1242/dev.083006 · Cited by 121
On the origin of the human germline
Kobayashi, T., & Surani, M. A. (2018) · Development · doi:10.1242/dev.150433 · Cited by 115
A critical role of PRDM14 in human primordial germ cell fate revealed by inducible degrons
Sybirna, A., Tang, W. W. C., Smela, M. P., Dietmann, S., Gruhn, W. H., Brosh, R., & Surani, M. A. (2020) · Nature Communications · doi:10.1038/s41467-020-15042-0 · Cited by 115
Specific Immune Cell and Cytokine Characteristics of Human Testicular Germ Cell Neoplasia
Klein, B., Haggeney, T., Fietz, D., Indumathy, S., Loveland, K. L., Hedger, M., Kliesch, S., Weidner, W., Bergmann, M., & Schuppe, H.-C. (2016) · Human Reproduction · doi:10.1093/humrep/dew211 · Cited by 114
Pediatric Germ Cell Tumors: A Developmental Perspective
Pierce, J. L., Frazier, A. L., & Amatruda, J. F. (2018) · Advances in Urology · doi:10.1155/2018/9059382 · Cited by 96
Gilbert, D. C., Chandler, I. R., McIntyre, A., Goddard, N. C., Gabe, R., Huddart, R. A., & SHIPLEY, J. M. (2008) · The Journal of Pathology · doi:10.1002/path.2436 · Cited by 87
Differential Expression of SOX2 and SOX17 in Testicular Germ Cell Tumors
Nonaka, D. (2009) · American Journal of Clinical Pathology · doi:10.1309/ajcp7mncnbcrn8no · Cited by 85
Nettersheim, D., Heukamp, L. C., Fronhoffs, F., Grewe, M. J., Haas, N., Waha, A., Honecker, F. U., Waha, A., Kristiansen, G., & Schorle, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082881 · Cited by 84
Self-citationTesticular dysgenesis syndrome and the origin of carcinoma in situ testis
Sonne, S. B., Kristensen, D. M., Novotny, G. W., Olesen, I. A., Nielsen, J. E., Skakkebæk, N. E., Meyts, E. R., & Leffers, H. C. B. (2008) · International Journal of Andrology · doi:10.1111/j.1365-2605.2007.00855.x · Cited by 77
Nettersheim, D., Jostes, S., Sharma, R. K., Schneider, S., Hofmann, A., Ferreira, H. J., Hoffmann, P., Kristiansen, G., Esteller, M., & Schorle, H. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005415 · Cited by 74
Self-citationNettersheim, D., Berger, D., Jostes, S., Kristiansen, G., Lochnit, G., & Schorle, H. (2019) · Andrology · doi:10.1111/andr.12612 · Cited by 72
Self-citationThe mammalian germline as a pluripotency cycle
Leitch, H. G., & Smith, A. G. (2013) · Development · doi:10.1242/dev.091603 · Cited by 71
Malignant germ cell tumours of childhood: new associations of genomic imbalance
on behalf of the Children's Cancer and Leukaemia Group (CCLG), Palmer, R. D., Foster, N. A., Vowler, S. L., Roberts, I. S. D., Thornton, C. M., Hale, J., Schneider, D. T., Nicholson, J. C., & Coleman, N. (2007) · British Journal of Cancer · doi:10.1038/sj.bjc.6603602 · Cited by 71
Tracing the transitions from pluripotency to germ cell fate with CRISPR screening
Hackett, J. A., Huang, Y., Günesdogan, U., Gretarsson, K. H., Kobayashi, T., & Surani, M. A. (2018) · Nature Communications · doi:10.1038/s41467-018-06230-0 · Cited by 70
The epigenome of testicular germ cell tumors
Lind, G. E., Skotheim, R. I., & Lothe, R. A. (2007) · Apmis · doi:10.1111/j.1600-0463.2007.apm_660.xml.x · Cited by 69
Lobo, J., Costa, A. L., Cantante, M., Guimarães, R., Lopes, P., Antunes, L., Braga, I. C., Oliveira, J., Pelizzola, M., Henrique, R., et al. (2019) · Journal of Translational Medicine · doi:10.1186/s12967-019-1837-z · Cited by 66
Germ Cell Tumors in Adolescents and Young Adults
Fonseca, A., Frazier, A. L., & Shaikh, F. (2019) · Journal of Oncology Practice · doi:10.1200/jop.19.00190 · Cited by 66
Ji, P., Wang, X., Xie, N., & Li, Y. (2018) · Stem Cells International · doi:10.1155/2018/3256524 · Cited by 62
Killian, J. K., Dorssers, L. C. J., Trabert, B. L., Gillis, A., Cook, M. B., Wang, Y., Waterfall, J. J., Stevenson, H. S., Smith, W. I., Noyes, N., et al. (2016) · Genome Research · doi:10.1101/gr.201293.115 · Cited by 60
Licensing of Primordial Germ Cells for Gametogenesis Depends on Genital Ridge Signaling
Hu, Y., Nicholls, P. K., Soh, Y. Q. S., Daniele, J. R., Junker, J. P., van Oudenaarden, A., & Page, D. C. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005019 · Cited by 59
Nettersheim, D., Heimsoeth, A., Jostes, S., Schneider, S., Fellermeyer, M., Hofmann, A., & Schorle, H. (2016) · Oncotarget · doi:10.18632/oncotarget.9903 · Cited by 58
Self-citationMouse primordial germ cells use fibronectin as a substrate for migration
Álvarez-Buylla, A., & Merchant‐Larios, H. (1986) · Experimental Cell Research · doi:10.1016/0014-4827(86)90590-2 · Cited by 55
Fustino, N. J., Rakheja, D., Ateek, C., Neumann, J. C., & Amatruda, J. F. (2011) · International Journal of Andrology · doi:10.1111/j.1365-2605.2011.01186.x · Cited by 52
DNA Methylation Profiling as a Tool for Testicular Germ Cell Tumors Subtyping
Costa, A. L., Moreira-Barbosa, C., Lobo, J., Vilela-Salgueiro, B., Cantante, M., Guimarães, R., Lopes, P., Braga, I. C., Oliveira, J., Antunes, L., et al. (2018) · Epigenomics · doi:10.2217/epi-2018-0034 · Cited by 49
Kristensen, D. G., Skakkeb�k, N. E., Meyts, E. R., & Almstrup, K. (2013) · The International Journal of Developmental Biology · doi:10.1387/ijdb.130142ka · Cited by 47
Lei, T., Moos, S., Klug, J., Aslani, F., Bhushan, S., Wahle, E., Fröhlich, S., Meinhardt, A., & Fijak, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-22135-w · Cited by 46
Nettersheim, D., Gillis, A., Looijenga, L. H. J., & Schorle, H. (2011) · International Journal of Andrology · doi:10.1111/j.1365-2605.2011.01172.x · Cited by 45
Self-citationUnique and redundant roles of SOX2 and SOX17 in regulating the germ cell tumor fate
Jostes, S., Fellermeyer, M., Arévalo, L., et al. (2019) · International Journal of Cancer · doi:10.1002/ijc.32714 · Cited by 45
Nuclear Reprogramming in Mouse Primordial Germ Cells: Epigenetic Contribution
Felici, M. D. (2011) · Stem Cells International · doi:10.4061/2011/425863 · Cited by 44
Apoptosis Is a Demanding Selective Tool During the Development of Fetal Male Germ Cells
Bejarano, I., Rodríguez, A. B., & Pariente, J. A. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00065 · Cited by 41
Genomic Imprinting and Cancer: From Primordial Germ Cells to Somatic Cells
Murrell, A. (2006) · The Scientific World JOURNAL · doi:10.1100/tsw.2006.318 · Cited by 39
Lobo, J., Henrique, R., & Jerónimo, C. (2018) · Cancers · doi:10.3390/cancers11010006 · Cited by 35
Young, J. C., Jaiprakash, A. T., Mithraprabhu, S., Itman, C., Kitazawa, R., Looijenga, L. H. J., & Loveland, K. L. (2011) · International Journal of Andrology · doi:10.1111/j.1365-2605.2011.01170.x · Cited by 31
Testing the role of SOX15 in human primordial germ cell fate
Smela, M. P., Sybirna, A., Wong, F. C. K., & Surani, M. A. (2019) · Wellcome Open Research · doi:10.12688/wellcomeopenres.15381.2 · Cited by 30
Sun, X., Park, C. B., Deng, W., Potter, S. S., & Dey, S. K. (2015) · The FASEB Journal · doi:10.1096/fj.15-282798 · Cited by 28
Testing the role of SOX15 in human primordial germ cell fate
Smela, M. P., Sybirna, A., Wong, F. C. K., & Surani, M. A. (2019) · Wellcome Open Research · doi:10.12688/wellcomeopenres.15381.1 · Cited by 26
Nettersheim, D., Vadder, S., Jostes, S., Heimsoeth, A., & Schorle, H. (2019) · Cancers · doi:10.3390/cancers11050728 · Cited by 25
Self-citationSETDB1 is essential for mouse primordial germ cell fate determination by ensuring BMP signaling
Mochizuki, K., Tando, Y., Sekinaka, T., Otsuka, K., Hayashi, Y., Kobayashi, H., Kamio, A., Ito‐Matsuoka, Y., Takehara, A., Kono, T., et al. (2018) · Development · doi:10.1242/dev.164160 · Cited by 22
Epigenetic Signatures In Stem Cells And Cancer Stem Cells
Hernández‐Vargas, H., Sinčić, N., Ouzounova, M., & Herceg, Z. (2009) · Epigenomics · doi:10.2217/epi.09.19 · Cited by 21
Elucidating human male germ cell development by studying germ cell cancer
Nettersheim, D., Jostes, S., Schneider, S., & Schorle, H. (2016) · Reproduction · doi:10.1530/rep-16-0114 · Cited by 21
Self-citationOliveros, M., Li, Z., Nee, K., Hosohama, L., Calvopina, J. H., Lee, S. A., Joti, P., Yu, J., & Clark, A. T. (2015) · Stem Cell Reports · doi:10.1016/j.stemcr.2015.07.006 · Cited by 16
Li, H., Liang, R., Lu, Y., Wang, M., & Li, Z. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17040382 · Cited by 16
Szarek, M., Bergmann, M., Konrad, L., Schuppe, H. ‐., Kliesch, S., Hedger, M. P., & Loveland, K. L. (2018) · Andrology · doi:10.1111/andr.12553 · Cited by 13
Pathogenesis of Testicular Germ Cell Neoplasia: A Conceptual Approach
Baraban, E. G., & Cooper, K. (2019) · Advances in Anatomic Pathology · doi:10.1097/pap.0000000000000233 · Cited by 10
Krishnan, S. P. (2015) · TURKISH JOURNAL OF BIOLOGY · doi:10.3906/biy-1407-16 · Cited by 4
Cited by
Skowron, M. A., Eul, K., Stephan, A., Ludwig, G. F., Wakileh, G. A., Bister, A., Söhngen, C., Raba, K., Petzsch, P., Poschmann, G., et al. (2022) · Molecular Oncology · doi:10.1002/1878-0261.13282 · Cited by 20
Self-citationEvmorfopoulos, K., Marsitopoulos, K., Karachalios, R., Karathanasis, A., Dimitropoulos, K., Tzortzis, V., Zachos, I., & Vlachostergios, P. J. (2024) · Cancers · doi:10.3390/cancers16020428 · Cited by 11
“In TGCTs, the relationship between malignant cells and the surrounding tumor microenvironment (TME) seems to play an important role in the disruption of this balance [16–19].”
Background
Metadata
- Authors
- Müller, M. R., Skowron, M. A., Albers, P., & Nettersheim, D.
- Affiliations
- Düsseldorf University Hospital (DE)
- Corresponding author
- Nettersheim, Daniel
- Venue
- Asian Journal of Urology
- Publisher
- Elsevier BV
- Published
- 2021-04
- Volume
- 8
- Issue
- 2
- Pages
- 144-154
- ISSN
- 2214-3882 (ISSN-L)
- PMC
- PMC8099689
- OpenAlex
- W3030743858
- Cited by
- 50
- References
- 77
- Citations by year
- 2026: 11 · 2025: 8 · 2024: 11 · 2023: 10 · 2022: 7 · 2021: 3
- FWCI
- 1.13
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- cc-by-nc-nd
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- creativecommons.org/licenses/by-nc-nd/4.0/ (vor)
- Locations
- Asian journal of urology (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Health Sciences › Medicine › Surgery › Testicular diseases and treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Health Sciences › Medicine › Reproductive Medicine › Sperm and Testicular Function
- Keywords
- germ cell tumors, primordial germ cells, epigenetic modifications, SOX2, SOX17, embryonal carcinoma, seminoma, germ cell neoplasia in situ, BMP signaling, tumor microenvironment, pluripotency regulation, germ cell migration, tumor plasticity
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.