Establishment of a Human Multiple Myeloma Xenograft Model in the Chicken to Study Tumor Growth, Invasion and Angiogenesis

被引:14
|
作者
Martowicz, Agnieszka [1 ,4 ]
Kern, Johann [1 ,2 ]
Gunsilius, Eberhard [1 ]
Untergasser, Gerold [1 ,3 ]
机构
[1] Med Univ Innsbruck, Dept Internal Med 5, A-6020 Innsbruck, Austria
[2] Oncotyrol GmbH, Innsbruck, Austria
[3] Tyrolean Canc Res Inst, Innsbruck, Austria
[4] Karolinska Inst, Dept Med Biochem & Biophys, Div Vasc Biol, S-10401 Stockholm, Sweden
来源
基金
奥地利科学基金会;
关键词
Medicine; Issue; 99; CAM; angiogenesis; mesenchymal cells; multiple myeloma; GFP; 3-dimensional tissue culture; xenografts; tumor; CELLS; ENGRAFTMENT; THERAPY; MICE;
D O I
10.3791/52665
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multiple myeloma (MM), a malignant plasma cell disease, remains incurable and novel drugs are required to improve the prognosis of patients. Due to the lack of the bone microenvironment and auto/paracrine growth factors human MM cells are difficult to cultivate. Therefore, there is an urgent need to establish proper in vitro and in vivo culture systems to study the action of novel therapeutics on human MM cells. Here we present a model to grow human multiple myeloma cells in a complex 3D environment in vitro and in vivo. MM cell lines OPM-2 and RPMI-8226 were transfected to express the transgene GFP and were cultivated in the presence of human mesenchymal cells and collagen type-I matrix as three-dimensional spheroids. In addition, spheroids were grafted on the chorioallantoic membrane (CAM) of chicken embryos and tumor growth was monitored by stereo fluorescence microscopy. Both models allow the study of novel therapeutic drugs in a complex 3D environment and the quantification of the tumor cell mass after homogenization of grafts in a transgene-specific GFP-ELISA. Moreover, angiogenic responses of the host and invasion of tumor cells into the subjacent host tissue can be monitored daily by a stereo microscope and analyzed by immunohistochemical staining against human tumor cells (Ki-67, CD138, Vimentin) or host mural cells covering blood vessels (desmin/ASMA). In conclusion, the onplant system allows studying MM cell growth and angiogenesis in a complex 3D environment and enables screening for novel therapeutic compounds targeting survival and proliferation of MM cells.
引用
收藏
页数:9
相关论文
共 50 条
  • [31] Interleukin-12 inhibits tumor growth in a novel angiogenesis canine hemangiosarcoma xenograft model
    Akhtar, N
    Padilla, ML
    Dickerson, EB
    Steinberg, H
    Breen, M
    Auerbach, R
    Helfand, SC
    NEOPLASIA, 2004, 6 (02): : 106 - 116
  • [32] Syndecan-1 Overexpression Promotes Tumor Growth and Angiogenesis in an Endometrial Cancer Xenograft Model
    Oh, Jeong-Hyun
    Lee, Hae-Sun
    Park, Sang-Hyun
    Ryu, Hee-Sug
    Min, Churl K.
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2010, 20 (05) : 751 - 756
  • [33] A xenograft model reveals that PU.1 functions as a tumor suppressor for multiple myeloma in vivo
    Nishimura, Nao
    Endo, Shinya
    Ueno, Shikiko
    Ueno, Nina
    Tatetsu, Hiro
    Hirata, Shinya
    Hata, Hiroyuki
    Komohara, Yoshihiro
    Takeya, Motohiro
    Mitsuya, Hiroaki
    Okuno, Yutaka
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2017, 486 (04) : 916 - 922
  • [34] In vivo model for human tumor angiogenesis in leukemia/lymphoma or multiple myeloma and the tumor regression by anti-angiogenic gene therapy.
    Yamada, T
    Kondoh, K
    Hashiguchi, A
    Du, WL
    Hozumi, N
    Suda, T
    Sakamoto, M
    Hata, J
    BLOOD, 2002, 100 (11) : 562A - 562A
  • [35] VEGF Antibody Plus Cisplatin Reduces Angiogenesis and Tumor Growth in a Xenograft Model of Ovarian Cancer
    Ghosh, Sonali
    Maity, Putul
    JOURNAL OF ENVIRONMENTAL PATHOLOGY TOXICOLOGY AND ONCOLOGY, 2010, 29 (01) : 17 - 30
  • [36] ProstaCaid™ inhibits tumor growth in a xenograft model of human prostate cancer
    Jiang, Jiahua
    Loganathan, Jagadish
    Eliaz, Isaac
    Terry, Colin
    Sandusky, George E.
    Sliva, Daniel
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2012, 40 (05) : 1339 - 1344
  • [37] Angiogenesis, hypoxia and VEGF expression during tumour growth in a human xenograft tumour model
    Hendriksen, E. M.
    Span, P. N.
    Schuuring, J.
    Peters, J. P. W.
    Sweep, F. C. G. J.
    van der Kogel, A. J.
    Bussink, J.
    MICROVASCULAR RESEARCH, 2009, 77 (02) : 96 - 103
  • [38] Xenograft Models of Multiple Myeloma Reveal That PU.1 Serves As a Tumor Suppressor for Multiple Myeloma
    Nishimura, Nao
    Endo, Shinya
    Ueno, Niina
    Ueno, Shikiko
    Yuki, Hiromichi
    Hata, Hiroyuki
    Mitsuya, Hiroaki
    Okuno, Yutaka
    BLOOD, 2014, 124 (21)
  • [39] The Angiogenesis Inhibitor VEGF Trap (Aflibercept), a Soluble VEGF Decoy Receptor, Inhibits Tumor Growth in a Human HCC Xenograft Model
    Graepler, Florian
    Nissler, Valerie
    Scharpf, Marcus
    Vonthein, Reinhard
    Heidenreich, Regina
    Wehrmann, Manfred
    Rudge, John
    Bitzer, Michael
    Gregor, Michael
    Lauer, Ulrich M.
    GASTROENTEROLOGY, 2009, 136 (05) : A620 - A620
  • [40] Establishment of Patient-Derived Xenograft (PDX) Zebrafish Model of Multiple Myeloma and Its Application in Drug Screening
    Yu, Zhen
    Li, Ying
    Wang, Kefei
    Wang, Lu
    Qiu, Lugui
    Hao, Mu
    BLOOD, 2022, 140 : 12524 - 12524