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Cancer stem cells in osteosarcoma
Open accessAbstract
Osteosarcoma is the most common primary bone tumour in children and adolescents and advanced osteosarcoma patients with evidence of metastasis share a poor prognosis. Osteosarcoma frequently gains resistance to standard therapies highlighting the need for improved treatment regimens and identification of novel therapeutic targets. Cancer stem cells (CSC) represent a sub-type of tumour cells attributed to critical steps in cancer including tumour propagation, therapy resistance, recurrence and in some cases metastasis. Recent published work demonstrates evidence of cancer stem cell phenotypes in osteosarcoma with links to drug resistance and tumorigenesis. In this review we will discuss the commonly used isolation techniques for cancer stem cells in osteosarcoma as well as the identified biochemical and molecular markers.
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“This seed and soil phenomenon is driven by a microenvironment that modulates osteosarcoma cell behaviour and facilitates proliferation, quiescence, invasion, migration, and drug resistance 15,51,52,53 and contributes to their intrinsic heterogeneity 54,55 .”
From Osteosarcoma (2022) · cites this paper as [52]
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Cites
Single-cell RNA-seq highlights intratumoral heterogeneity in primary glioblastoma
Patel, A. P., Tirosh, I., Trombetta, J. J., Shalek, A. K., Gillespie, S. M., Wakimoto, H., Cahill, D. P., Nahed, B. V., Curry, W. T., Martuza, R. L., et al. (2014) · Science · doi:10.1126/science.1254257 · Cited by 5,063
Clarke, M. F., Dick, J. E., Dirks, P. B., Eaves, C., Jamieson, C., Jones, D. L., Visvader, J., Weissman, I. L., & Wahl, G. (2006) · Cancer Research · doi:10.1158/0008-5472.can-06-3126 · Cited by 3,124
Tumour evolution inferred by single-cell sequencing
Navin, N., Kendall, J., Troge, J., Andrews, P., Rodgers, L., McIndoo, J., Cook, K., Stepansky, A., Levy, D., Esposito, D., et al. (2011) · Nature · doi:10.1038/nature09807 · Cited by 2,598
Cancer stem cell definitions and terminology: the devil is in the details
Valent, P., Bonnet, D. A., Maria, R. D., Lapidot, T., Copland, M., Melo, J. V., Chomienne, C., Ishikawa, F., Schuringa, J. J., Stassi, G., et al. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3368 · Cited by 720
Mechanisms of Stem Cell Self-Renewal
He, S., Nakada, D., & Morrison, S. J. (2009) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.042308.113248 · Cited by 644
Stem-Like Cells in Bone Sarcomas: Implications for Tumorigenesis
Gibbs, C. P., Kukekov, V. G., Reith, J. D., Tchigrinova, O., Suslov, O. N., Scott, E. W., Ghivizzani, S. C., Ignatova, T. N., & Steindler, D. A. (2005) · Neoplasia · doi:10.1593/neo.05394 · Cited by 492
Tirino, V., Desiderio, V., Paino, F., ROSA, A. D., Papaccio, F., Noce, M. L., Laino, L., Francesco, F. D., & Papaccio, G. (2012) · The FASEB Journal · doi:10.1096/fj.12-218222 · Cited by 391
Exome sequencing of osteosarcoma reveals mutation signatures reminiscent of BRCA deficiency
Kovac, M., Blattmann, C., Ribi, S., Smida, J., Mueller, N. S., Engert, F., Castro-Giner, F., Weischenfeldt, J., Kovacova, M., Krieg, A., et al. (2015) · Nature Communications · doi:10.1038/ncomms9940 · Cited by 353
Detection and Characterization of CD133+ Cancer Stem Cells in Human Solid Tumours
Tirino, V., Desiderio, V., d’Aquino, R., Francesco, F. D., Pirozzi, G., Galderisi, U., Cavaliere, C., Rosa, A. D., & Papaccio, G. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003469 · Cited by 292
Kim, K., Lee, H. W., Lee, H., Kim, S. C., Seo, Y. J., Chung, W., Eum, H. H., Nam, D., Kim, J., Joo, K. M., et al. (2015) · Genome biology · doi:10.1186/s13059-015-0692-3 · Cited by 269
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Self-citationCancer stem cells: advances in knowledge and implications for cancer therapy
Chu, X., Tian, W., Ning, J., Xiao, G., Zhou, Y., Wang, Z., Zhai, Z., Tanzhu, G., Yang, J., & Zhou, R. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01851-y · Cited by 656
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Chen, C., Xie, L., Ren, T., Huang, Y., Xu, J. H., & Guo, W. (2020) · Cancer Letters · doi:10.1016/j.canlet.2020.12.024 · Cited by 587
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Czarnecka, A. M., Synoradzki, K. J., Firlej, W., Bartnik, E., Sobczuk, P., Fiedorowicz, M., Grieb, P., & Rutkowski, P. L. (2020) · Cancers · doi:10.3390/cancers12082130 · Cited by 343
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Grünewald, T. G., Alonso, M., Avnet, S., Banito, A., Burdach, S., Cidre‐Aranaz, F., Di Pompo, G., Distel, M., Dorado‐Garcia, H., Garcia‐Castro, J., et al. (2020) · EMBO Molecular Medicine · doi:10.15252/emmm.201911131 · Cited by 319
Self-citationAdvances on immunotherapy for osteosarcoma
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“Cancer stem cells (CSCs) CSCs are a subset of tumor cells that play a pivotal role in various stages of cancer development, including tumorigenesis, drug resistance, recurrence and metastasis [43, 44].”
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Deng, B., Zhao, Z., Kong, W., Han, C., Shen, X., & Zhou, C. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03768-y · Cited by 278
Heymann, M.-F., Lézot, F., & Heymann, D. (2019) · Cellular Immunology · doi:10.1016/j.cellimm.2017.10.011 · Cited by 233
Self-citationOsteosarcoma mechanobiology and therapeutic targets
Shoaib, Z., Fan, T. M., & Irudayaraj, J. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15713 · Cited by 239
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Tang, L., Xiao, Q., Mei, Y., He, S., Zhang, Z., Wang, R., & Wang, W. (2021) · Journal of Nanobiotechnology · doi:10.1186/s12951-021-01174-y · Cited by 191
Dormant, quiescent, tolerant and persister cells: Four synonyms for the same target in cancer
Vallette, F. M., Olivier, C., Lézot, F., Oliver, L., Cochonneau, D., Lalier-Bretaudeau, L., Cartron, P., & Heymann, D. (2018) · Biochemical Pharmacology · doi:10.1016/j.bcp.2018.11.004 · Cited by 192
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Lin, H., Chen, X., Zhang, C., Yang, T., Deng, Z., Song, Y., Huang, L. J., Li, F., Li, Q., Lin, S., et al. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.111202 · Cited by 176
Mesenchymal stroma: Role in osteosarcoma progression
Cortini, M., Avnet, S., & Baldini, N. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.07.024 · Cited by 171
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Brown, H. K., Schiavone, K., Gouin, F., Heymann, M.-F., & Heymann, D. (2018) · Calcified Tissue International · doi:10.1007/s00223-017-0372-2 · Cited by 163
Self-citationZhang, X., Powell, K. A., & Li, L. (2020) · Cancers · doi:10.3390/cancers12123765 · Cited by 163
Jones, C. L., Sheth, A. I., & Jordan, C. T. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.02.013 · Cited by 166
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Mierke, C. T. (2024) · Cells · doi:10.3390/cells13010096 · Cited by 146
Panez-Toro, I., Muñoz-García, J., Vargas-Franco, J. W., Renodon‐Cornière, A., Heymann, M., Lézot, F., & Heymann, D. (2023) · Current Osteoporosis Reports · doi:10.1007/s11914-023-00803-9 · Cited by 133
Self-citationZebrafish xenograft models of cancer and metastasis for drug discovery
Brown, H. K., Schiavone, K., Tazzyman, S. J., Heymann, D., & Chico, T. (2017) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2017.1297416 · Cited by 130
Self-citationÁlvarez, C., Monasterio, G., Cavalla, F., Córdova, L. A., Hernández, M., Heymann, D., Garlet, G. P., Sorsa, T. A., Pärnänen, P., Lee, H., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01664 · Cited by 116
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Liu, H., Gao, X., & Hou, Y. (2019) · Brazilian Journal of Psychiatry · doi:10.1590/1516-4446-2018-0346 · Cited by 101
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Ma, Z., Shuai, Y., Gao, X., Wen, X., & Ji, J. (2020) · Molecular Cancer · doi:10.1186/s12943-019-1113-0 · Cited by 96
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Bassi, G., Panseri, S., Dozio, S. M., Sandri, M., Campodoni, E., Dapporto, M., Sprio, S., Tampieri, A., & Montesi, M. (2020) · Scientific Reports · doi:10.1038/s41598-020-79448-y · Cited by 101
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Wang, Y., Zeng, L., Liang, C., Zan, R., Ji, W., Zhang, Z., Wei, Y., Tu, S., & Dong, Y. (2019) · Epigenomics · doi:10.2217/epi-2019-0262 · Cited by 73
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Liang, L., & Kaufmann, A. M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032555 · Cited by 66
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Chen, C., Zhang, L., Jiao, Y., Zhou, Y., Ge, Q., Li, P., Sun, X., & Lv, Z. (2019) · FEBS Letters · doi:10.1002/1873-3468.13387 · Cited by 56
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Schiavone, K., Garnier, D., Heymann, M., & Heymann, D. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-14366-4_11 · Cited by 55
Self-citationDai, J., Qin, L., Chen, Y., Wang, H., Lin, G., Li, X., Liao, H., & Fang, H. (2018) · Journal of the mechanical behavior of biomedical materials/Journal of mechanical behavior of biomedical materials · doi:10.1016/j.jmbbm.2018.10.012 · Cited by 56
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Wang, S., Hu, H., Zhong, B., Shi, D., Qing, X., Cheng, C., Deng, X., Zhang, Z., & Shao, Z. (2019) · Cancer Medicine · doi:10.1002/cam4.2612 · Cited by 48
Lu, B., He, Y., He, J., Wang, L., Liu, Z., Yang, J., Gao, Z., Lu, G., Zou, C., & Zhao, W. (2019) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-19-0470 · Cited by 48
Chen, Y., Wang, T., Huang, M., Liu, Q., Hu, C., Wang, B., Han, D. H., Chen, C. Y., Zhang, J., Li, Z., et al. (2020) · Cancer Research · doi:10.1158/0008-5472.can-19-1764 · Cited by 48
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Liu, J., & Shang, G. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.773038 · Cited by 47
Takahashi, N., Nobusue, H., Shimizu, T., Sugihara, E., Yamaguchi‐Iwai, S., Onishi, N., Kunitomi, H., Kuroda, T., & Saya, H. (2019) · Cancer Research · doi:10.1158/0008-5472.can-18-2693 · Cited by 47
Qi, J., Zhang, R., & Wang, Y. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17024 · Cited by 47
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Gilbert, A., Tudor, M., Montanari, J., Commenchail, K., Savu, D., Lesueur, P., & Chevalier, F. (2023) · Cancers · doi:10.3390/cancers15071962 · Cited by 51
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Zhao, D., Wang, S., Chu, X., & Han, D. (2019) · Artificial Cells Nanomedicine and Biotechnology · doi:10.1080/21691401.2019.1596934 · Cited by 44
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Sun, X., Tian, C., Zhang, H., Han, K., Zhou, M., Gan, Z., Zhu, H., & Min, D. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110201 · Cited by 41
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Zhang, H., Wang, T., Gong, H., Jiang, R., Wang, Z., Sun, H., Huang, R., Wang, Y., Wu, Z., Xu, W., et al. (2023) · Bone Research · doi:10.1038/s41413-022-00233-w · Cited by 41
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Xu, S., Gong, Y., Yin, Y., Xing, H., & Zhang, N. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110141 · Cited by 40
Li, R., Ruan, Q., Zheng, J., Zhang, B., & Yang, H. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.632206 · Cited by 40
Zhang, Z., Pu, F., Wang, B., Wu, Q., Liu, J., & Shao, Z. (2019) · Gene Therapy · doi:10.1038/s41434-019-0112-5 · Cited by 39
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Gatti, M., Solari, A., Pattarozzi, A., Campanella, C., Thellung, S., Maniscalco, L., Maria, R. D., Würth, R., Corsaro, A., Bajetto, A., et al. (2018) · Experimental Cell Research · doi:10.1016/j.yexcr.2018.01.002 · Cited by 39
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Ruan, X., Jin, X., Sun, F., Pi, J., Jinghu, Y., Lin, X., Zhang, N., & Chen, G. (2024) · The FASEB Journal · doi:10.1096/fj.202401298r · Cited by 40
Ye, G., Huang, M., Li, Y., Ouyang, J., Chen, M., Wen, Q., Li, X., Zeng, H.-H., Long, P., Fan, Z., et al. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.08.015 · Cited by 37
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Zhao, Y., Zhang, B., Zhang, Q., Ma, X., & Feng, H. (2021) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b2100029 · Cited by 37
Yang, B., Su, Z., Chen, G., Zeng, Z., Tan, J., Wu, G., Zhu, S., & Lin, L. (2021) · Oncology Letters · doi:10.3892/ol.2021.12441 · Cited by 36
Freeman, F. E., Burdis, R., Mahon, O. R., Kelly, D. J., & Artzi, N. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202101296 · Cited by 36
Tian, Z., Wang, J. Q., & Ge, H. (2019) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2019.07.003 · Cited by 34
Menéndez, S. T., Rey, V., Martínez-Cruzado, L., González, M. V., Morales‐Molina, Á., Santos, L. M., Blanco, V., Álvarez-Fernández, C., Estupiñán, Ó., Allonca, E., et al. (2020) · Cancers · doi:10.2139/ssrn.3520041 · Cited by 31
Pereira‐Silva, M., Alvarez‐Lorenzo, C., Concheiro, Á., Paiva‐Santos, A. C., Veiga, F., & Figueiras, A. (2020) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2019.10.013 · Cited by 32
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Perkins, R. S., Murray, G., Suthon, S., Davis, L., Perkins, N. B., Fletcher, L. B., Bozzi, A., Schreiber, S. L., Lin, J., Laxton, S. J., et al. (2024) · Clinical and Translational Medicine · doi:10.1002/ctm2.1670 · Cited by 30
Sun, F., Zhang, Y., Xu, L., Li, S., Chen, X. '., Zhang, L., Wu, Y., & Li, J. (2017) · Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics · doi:10.3727/096504017x15119525209765 · Cited by 30
Bu, J., Guo, R., Xu, X.-Z., Luo, Y., & Liu, J. (2021) · Journal of bone oncology · doi:10.1016/j.jbo.2021.100348 · Cited by 30
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Shi, X., Li, X., Wang, H., Yu, Z., Zhu, Y., & Gao, Y. (2018) · Journal of bone oncology · doi:10.1016/j.jbo.2018.11.001 · Cited by 29
Pompo, G. D., Cortini, M., Palomba, R., Francesco, V. D., Bellotti, E., Decuzzi, P., Baldini, N., & Avnet, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115760 · Cited by 29
Guo, J., Tang, H., Huang, P., Guo, J., Shi, Y., Yuan, C., Liang, T., & Tang, K. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.732862 · Cited by 28
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Robin, P., Singh, K., & Suntharalingam, K. (2019) · Chemical Communications · doi:10.1039/c9cc08962d · Cited by 28
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Chao, C., Lee, W.-F., Yang, W., Lin, C., Han, C., Huang, Y., Fong, Y., Wu, M., Lee, I., Tsai, Y.-H., et al. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118758 · Cited by 28
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Liu, B., Li, C., He, S., Li, Z., Wang, H., Feng, C., Xiong, Z., Tu, C., Song, D., & Li, Z. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114545 · Cited by 25
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Liu, J., Lee, C., Lin, C., Chao, C., Chang, T., Han, C.-K., Huang, Y., Fong, Y., & Tang, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21176095 · Cited by 25
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Tsang, S. V., Rainusso, N. C., Liu, M., Nomura, M., Patel, T. D., Nakahata, K., Kim, H. R., Huang, S., Rajapakshe, K., Coarfa, C., et al. (2022) · Oncogene · doi:10.1038/s41388-022-02538-w · Cited by 25
Benslimane-Ahmim, Z., Pereira, J. R. D. S., Lokajczyk, A., Dizier, B., Galy–Fauroux, I., Fischer, A., Heymann, D., & Boisson‐Vidal, C. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.02.032 · Cited by 25
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Wang, J., Zhou, J., Xie, Z., Zhang, Y., He, M., Wei, T., Wu, S., & Du, C. (2025) · Biofabrication · doi:10.1088/1758-5090/adc29e · Cited by 23
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Han, X., Yang, S., Mo, H., Wang, M., Zhou, F., Li, H., Qiao, H., Mei, J., Wang, Y., Cheng, Y., et al. (2019) · Advanced Functional Materials · doi:10.1002/adfm.201902246 · Cited by 23
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Chaojian, L., Cai, L., & Li, H. (2019) · Molecular Medicine Reports · doi:10.3892/mmr.2019.10534 · Cited by 23
Targeting LRP6: A new strategy for cancer therapy
Xue, W., Zhu, B., Zhao, K., Huang, Q., Luo, H., Shou, Y., Huang, Z., & Guo, H. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107200 · Cited by 22
Varès, G., Ahire, V. R., Sunada, S., Kim, E. H., Sai, S., Chevalier, F., Roméo, P., Yamamoto, T. S., Nakajima, T., & Saintigny, Y. (2020) · Radiotherapy and Oncology · doi:10.1016/j.radonc.2020.07.034 · Cited by 22
Yang, J., Hu, Y., Wang, L., Sun, X., Yu, L., & Guo, W. (2021) · Bioengineered · doi:10.1080/21655979.2021.2005220 · Cited by 22
Wang, W. T., & Wang, B. (2022) · BMC Cancer · doi:10.1186/s12885-022-09636-8 · Cited by 22
Chen, Z., Huang, H., Li, Q., Zhan, F., Wang, L.-B., He, T., Yang, C., Wang, Y., Zhang, Y., & Quan, Z. (2023) · The American Journal of Chinese Medicine · doi:10.1142/s0192415x23500489 · Cited by 22
Metadata
- Authors
- Brown, H. K., Tellez-Gabriel, M., & Heymann, D.
- Affiliations
- Inserm (FR)
- Corresponding author
- Brown, Hannah K.
- Heymann, Dominique
- ORCID
- Heymann, Dominique
- Venue
- Cancer Letters
- Publisher
- Elsevier BV
- Published
- 2017-02
- Volume
- 386
- Pages
- 189-195
- ISSN
- 0304-3835 (ISSN-L)
- OpenAlex
- W2551783204
- Cited by
- 303
- References
- 47
- Citations by year
- 2026: 12 · 2025: 23 · 2024: 43 · 2023: 33 · 2022: 41 · 2021: 49 · 2020: 50 · 2019: 34 · 2018: 10 · 2017: 8
- FWCI
- 1.74
- Type
- journal article
- Language
- en
- Open access
- green
- inserm.hal.science
- Licence
- Locations
- Cancer Letters (publishedVersion)
- PubMed (publishedVersion)
- White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (acceptedVersion)
- HAL (submittedVersion, other-oa)
- Funders
- Bone Cancer Research Trust (144681)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Health Sciences › Medicine › Oncology › Sarcoma Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Keywords
- osteosarcoma, cancer stem cells, drug resistance, carcinogenesis, metastasis, cancer stem cell isolation, molecular markers, therapeutic target, pediatric bone tumors
- MeSH terms
- Animals, Antineoplastic Agents, Bone Neoplasms, Cell Separation, Humans, Phenotype, Osteosarcoma, Biomarkers, Tumor, Neoplastic Stem Cells, Drug Resistance, Neoplasm
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