Eribulin Regresses a Cisplatinum-resistant Rare-type Triple-negative Matrix-producing Breast Carcinoma Patient-derived Orthotopic Xenograft Mouse Model

被引:9
|
作者
Yamamoto, Jun [1 ,2 ,3 ]
Murata, Takuya [4 ]
Sugisawa, Norihiko [1 ,2 ]
Higuchi, Takashi [1 ,2 ]
Tashiro, Yoshihiko [1 ,2 ]
Nishino, Hiroto [1 ,2 ]
Inubushi, Sachiko [1 ,2 ]
Sun, Yu [1 ,2 ]
Lim, Hyein [1 ,2 ]
Miyake, Kentaro [3 ]
Shimoya, Koichiro [5 ]
Nomura, Tsunehisa [6 ]
Kurebayashi, Junichi [6 ]
Tanino, Hirokazu [7 ]
Hozumi, Chihiro [8 ]
Bouvet, Michael [2 ]
Singh, Shree Ram [9 ]
Endo, Itaru [3 ]
Hoffman, Robert M. [1 ]
机构
[1] AntiCancer Inc, 7917 Ostrow St, San Diego, CA 92111 USA
[2] Univ Calif San Diego, Dept Surg, San Diego, CA 92103 USA
[3] Yokohama City Univ, Grad Sch Med, Dept Gastroenterol Surg, Yokohama, Kanagawa, Japan
[4] Kawasaki Med Sch, Dept Obstet & Gynecol 2, Okayama, Japan
[5] Kawasaki Med Sch, Dept Obstet & Gynecol 1, Kurashiki, Okayama, Japan
[6] Kawasaki Med Sch, Dept Breast & Thyroid Surg, Kurashiki, Okayama, Japan
[7] Kobe Univ, Grad Sch Med, Dept Surg, Breast Surg, Kobe, Hyogo, Japan
[8] AntiCancer Japan Inc, Narita, Japan
[9] Natl Canc Inst, Basic Res Lab, Frederick, MD 21702 USA
关键词
PDOX; patient-derived orthotopic xenograft; TNBC; triple-negative breast cancer; matrix-producing breast carcinoma; eribulin; cisplatinum; tumor regression; CANCER; FEATURES; OSTEOSARCOMA; METASTASIS; SURVIVAL;
D O I
10.21873/anticanres.14217
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Matrix-producing breast carcinoma (MPBC) is a rare and usually aggressive triple-negative breast cancer (TNBC). In the present report, we determined the drug sensitivity for a triple-negative MPBC using a patient-derived orthotopic xenograft (PDOX) model. Materials and Methods: The PDOX model was established in the left 2nd mammary by surgical orthotopic implantation (SOI). MPBC PDOX models were randomized into 4 groups (6 mice per group) when the tumor volume became 80 mm(3): G1, control group; G2, cisplatinum group [intraperitoneal (i.p.) injection, weekly, for 2 weeks]; G3, paclitaxel group (i.p., weekly, for 2 weeks); G4, eribulin group [intravenous (i.v.) injection, weekly, for 2 weeks]. All mice were sacrificed on day 15. Tumor volume and body weight were measured one time per week. Results: The MPBC PDOX model was resistant to cisplatinum (p=0.800). Paclitaxel suppressed tumor growth compared to the control group (p=0.009). However, only eribulin regressed the tumor (p=0.001). Conclusion: Eribulin has clinical potential for triple-negative MPBC patients.
引用
收藏
页码:2475 / 2479
页数:5
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