Cited by 37Sarcoma Diagnosis and TreatmentBone Tumor Diagnosis and TreatmentsCancer Cells and Metastasis

Establishment and characteristics of two syngeneic human osteosarcoma cell lines from primary tumor and skip metastases

ZOU, Chang-ye, WANG, Jin, SHEN, Jing-nan, HUANG, Gang, JIN, Song, YIN, Jun-qiang, GUO, Qian-chen, LI, Hao-miao +3 more·2008·Acta Pharmacologica Sinica

Abstract

Aim To characterize and compare the different biological behaviors of 2 novel human osteosarcoma cell lines, Zos and Zos-M, established respectively from the primary tumor and the skip metastasis of an osteosarcoma patient. Methods In vitro studies included morphological observations, karyotype analysis, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide cell proliferation assay, and cell sensitivity to chemotherapeutic drugs. Subcutaneous and intravenous inoculations into nude mice were carried out to study the tumorigenicity and the metastatic potential. RT-PCR was performed to assess the expression of the osteoblastic markers and some metastasis-related genes. Results Both cell lines remained stable for more than 100 passages in vitro without interruption. The RT-PCR examination indicated that they retained the molecular characteristics of an osteoblastic lineage. The karyotype analysis displayed aneuploidy and various structural abnormalities. Both cell lines are tumorigenic; Zos-M differs from Zos by the former's ability to develop lung metastasis after intravenous injection. The comparison of the expression patterns of some metastasis-related genes revealed that the decreased expression of cadherin-11 in Zos-M may correlate with a high potential of metastases. Moreover, both cell lines are less sensitive to the current chemotherapy protocols. Conclusion The establishment of osteosarcoma cell lines, Zos and Zos-M, and related animal models provide a useful reso…

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Crossref · 10.1111/j.1745-7254.2008.00756.x

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Authors
ZOU, C.-Y., WANG, J., SHEN, J.-N., HUANG, G., JIN, S., YIN, J.-Q., GUO, Q.-C., LI, H.-M., LUO, L., ZHANG, M., & ZHANG, L.-J.
Affiliations
Sun Yat-sen University (CN)
Venue
Acta Pharmacologica Sinica
Published
2008-03
Volume
29
Issue
3
Pages
325-332
ISSN
  • 0253-9756 (ISSN-L)
  • 1671-4083
  • 1745-7254
OpenAlex
W2037396413
Cited by
37
References
1
Citations by year
2026: 1 · 2025: 3 · 2024: 5 · 2023: 1 · 2022: 3 · 2021: 2 · 2020: 2 · 2018: 3 · 2017: 2 · 2016: 2 · 2015: 2 · 2014: 2 · 2013: 2 · 2012: 2
FWCI
1.22
Type
journal article
Language
en
Open access
closed
Locations
  • Acta Pharmacologica Sinica (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Natural Science Foundation of China (30200285)
  • Sun Yat-sen University
  • University of Texas MD Anderson Cancer Center
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Sarcoma Diagnosis and Treatment
  • Health Sciences › Medicine › Rheumatology › Bone Tumor Diagnosis and Treatments
  • Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
Keywords
osteosarcoma, skip metastasis, lung metastasis, cadherin-11, chemoresistance, tumorigenicity, metastasis-related gene expression, nude mouse xenograft
MeSH terms
Adolescent, Animals, Antimetabolites, Antineoplastic, Collagen, Drug Combinations, Extracellular Matrix, Formazans, Humans, Karyotyping, Laminin, Male, Methotrexate, Mice, Nude, Neoplasm Metastasis, Proteoglycans, Osteosarcoma, Tetrazolium Salts, Biomarkers, Tumor, Cell Lineage, Inhibitory Concentration 50, Xenograft Model Antitumor Assays, Cell Line, Tumor, Cell Proliferation, Mice

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