The reaction of bone to tumor growth from human breast cancer cells in a rat spine single metastasis model

Haixiang Liang, Shen Ying Ma, Khalid Mohammad, Theresa Guise, Gary Balian, Francis H. Shen

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

STUDY DESIGN. In vivo experiments to develop a rat spine single metastasis model by using human breast cancer cells. OBJECTIVE. To study the survival and tumorigenesis of the human breast cancer cells after transplantation to vertebral body (VB) by intraosseous injection as a model for therapeutic studies of spine metastatic tumor. SUMMARY OF BACKGROUND DATA. VBs are the most common bones involved in the metastases of breast cancer. To develop experimental therapeutics requires an appropriate animal model. Moreover, it is also important to establish accurate and sensitive detection methods for the evaluation. METHODS. MDA-MB-231 human breast cancer cells were injected into 3-week-old female athymic rats. The tumorigenesis was assayed with quantitative in vivo bioluminescence (IVIS), microcomputed tomography (micro-CT), quantitative CT (qCT), micro position emission tomography (micro-PET), and histologic studies. RESULTS. A spine single metastasis model of human breast cancer was successfully developed in rats. The IVIS signal intensity from the cancer cells increased after 2 weeks. Signal from the tumor in spine can be detected by micro-PET at day 1. The signal intensity decreased after 1 week and then recovered and continually increased afterwards. Bone destruction was demonstrated in the qCT and micro-CT images. However, both qCT and micro-CT found that the bone density in the cancer cell-injected VB increased before the appearance of osteolysis. The growth of tumor and the reaction of bone in the VB were observed simultaneously by histology. CONCLUSION. A spine single metastasis model was developed by injection of human breast cancer cells into the VB of athymic rats. This is the first report of quantitative evaluation with micro-PET in a spine metastasis model. In addition, the detection of osteogenesis after the introduction of MDA-MB-231 cells in vivo is a novel observation.

Original languageEnglish (US)
Pages (from-to)497-504
Number of pages8
JournalSpine
Volume36
Issue number7
DOIs
StatePublished - Apr 1 2011
Externally publishedYes

Fingerprint

Spine
Breast Neoplasms
Neoplasm Metastasis
Bone and Bones
X-Ray Microtomography
Growth
Nude Rats
Neoplasms
Tomography
Carcinogenesis
Osteolysis
Injections
Cell Transplantation
Osteogenesis
Bone Density
Histology
Animal Models
Observation
Survival
Therapeutics

Keywords

  • animal model
  • breast cancer
  • metastasis
  • positron emission tomography
  • spine tumor

ASJC Scopus subject areas

  • Clinical Neurology
  • Orthopedics and Sports Medicine

Cite this

The reaction of bone to tumor growth from human breast cancer cells in a rat spine single metastasis model. / Liang, Haixiang; Ma, Shen Ying; Mohammad, Khalid; Guise, Theresa; Balian, Gary; Shen, Francis H.

In: Spine, Vol. 36, No. 7, 01.04.2011, p. 497-504.

Research output: Contribution to journalArticle

Liang, Haixiang ; Ma, Shen Ying ; Mohammad, Khalid ; Guise, Theresa ; Balian, Gary ; Shen, Francis H. / The reaction of bone to tumor growth from human breast cancer cells in a rat spine single metastasis model. In: Spine. 2011 ; Vol. 36, No. 7. pp. 497-504.
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abstract = "STUDY DESIGN. In vivo experiments to develop a rat spine single metastasis model by using human breast cancer cells. OBJECTIVE. To study the survival and tumorigenesis of the human breast cancer cells after transplantation to vertebral body (VB) by intraosseous injection as a model for therapeutic studies of spine metastatic tumor. SUMMARY OF BACKGROUND DATA. VBs are the most common bones involved in the metastases of breast cancer. To develop experimental therapeutics requires an appropriate animal model. Moreover, it is also important to establish accurate and sensitive detection methods for the evaluation. METHODS. MDA-MB-231 human breast cancer cells were injected into 3-week-old female athymic rats. The tumorigenesis was assayed with quantitative in vivo bioluminescence (IVIS), microcomputed tomography (micro-CT), quantitative CT (qCT), micro position emission tomography (micro-PET), and histologic studies. RESULTS. A spine single metastasis model of human breast cancer was successfully developed in rats. The IVIS signal intensity from the cancer cells increased after 2 weeks. Signal from the tumor in spine can be detected by micro-PET at day 1. The signal intensity decreased after 1 week and then recovered and continually increased afterwards. Bone destruction was demonstrated in the qCT and micro-CT images. However, both qCT and micro-CT found that the bone density in the cancer cell-injected VB increased before the appearance of osteolysis. The growth of tumor and the reaction of bone in the VB were observed simultaneously by histology. CONCLUSION. A spine single metastasis model was developed by injection of human breast cancer cells into the VB of athymic rats. This is the first report of quantitative evaluation with micro-PET in a spine metastasis model. In addition, the detection of osteogenesis after the introduction of MDA-MB-231 cells in vivo is a novel observation.",
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