Hyaluronan expression in primary and secondary brain tumors

被引:19
|
作者
Jadin, Laurence [1 ]
Pastorino, Sandra [2 ]
Symons, Rebecca [1 ]
Nomura, Natsuko [2 ]
Jiang, Ping [1 ]
Juarez, Tiffany [2 ]
Makale, Milan [2 ]
Kesari, Santosh [2 ,3 ]
机构
[1] Halozyme Therapeut Inc, San Diego, CA USA
[2] Moores Canc Ctr, Translat Neuro Oncol Labs, 3855 Hlth Sci Dr,MC 0819, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
关键词
Hyaluronan (HA); breast cancer; glioblastoma (GBM); primary brain tumor; secondary brain tumor;
D O I
10.3978/j.issn.2305-5839.2015.04.07
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Collectively, primary and secondary brain tumors represent a major public health challenge. Glioblastoma (GBM) is the most common primary brain tumor in adults and is associated with a dismal 5-year survival of only 10%. Breast cancer causes secondary tumors; it occurs in 200,000 patients yearly and 30% of these individuals develop brain metastases which also lead to a very poor prognosis. GBM and primary breast tumors are known to express hyaluronan (HA) which may serve as a therapeutic target. Methods: For the present study we had two aims: (I) to identify suitable preclinical models for HA in GBM by examining HA expression in human GBM cell lines implanted orthotopically in mice; and (II) to determine whether breast cancer brain metastases in human patients express HA similar to the primary tumor. Forty human surgical samples of primary breast tumors and breast cancer brain metastases were processed and stained for HA. Athymic nu/nu mice were orthotopically implanted with one of 15 GBM lines and after tumors were established, quantitative immunohistochemistry determined whether. Results: HA was expressed. All GBM cell lines and patient-derived orthotopic tumors did express HA, with 3 primary human lines expressing the highest staining intensity, above that of normal brain. All 40 human primary breast tumors and brain metastases examined also contained HA, though staining intensity was highly variable. Conclusions: Our data support the use of specific patient-derived GBM cell lines in nu/nu mice for preclinical studies on HA-targeting therapies. Additionally, our research provides a basis for the assessment of HA expression and HA-targeting therapeutic agents for the treatment of breast cancer brain metastases.
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页数:8
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