Understanding the consequences of intratumor heterogeneity in sensitivity to antineoplastic drugs both in regard to the immediate effect on therapy and to longer term development of drug resistance, is of clear importance to effective therapy of human cancer. In order to study these consequences, we have developed a tumor model system, consisting of a series of mouse mammary tumor subpopulation lines and sublines, that are differentially sensitive to chemotherapeutic drugs. One of the major conclusions of our work thus far is that tumor subpopulations may alter each other's sensitivity to therapeutic drugs so that the drug response of a heterogeneous tumor is not simply the """"""""sum"""""""" of that of its component parts. We propose to investigate the mechanisms and consequences of this finding by reconstructing heterogeneous tumors using mixing paired subpopulations that differ in chemosensitivity and in ability to interact with each other.
Our first aim i s to examine the significance of heterogeneity on in vivo sensitivity to single chemotherapeutic drugs. Mechanisms by which heterogeneity can affect drug sensitivity will be elucidated by various in vivo techniques, including manipulation of growth parameters by the use of different tumor cell dosages and/or sites of injection, use of immunosuppressed mice, and use of related drugs which have different known properties (such as trimetrexate vs methotrexate). Interactions will be modeled in vitro so that mechanisms can be further ascertained, using the collagen gel culture system, which mimics the in vivo situation in that cells have maximum ability to interact with each other and display other similarities such as microenvironmental effects and growth/cell cycle characteristics.
Our second aim i s to analyse the significance of heterogeneity at different treatment times, including treating during primary tumor growth and after surgery as an adjuvant procedure. All tumors which are produced in experiments described above, will be analysed for the presence, physical distribution (zonality) and chemosensitivity of their component tumor subpopulations, using colony forming assays in selective media to identify and quantitate the populations (Aim 3). In order to better understand the basis for decreased drug sensitivity of tumor cells in our in vitro model of tumor cell growth, the collagen culture system, we will focus on differences in recovery from drug treatment in collagen cultures vs monolayer. The importance of factors such as growth rate and cell shape in affecting recovery will be determined (Aim 4).

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA027419-11
Application #
3167622
Study Section
Experimental Therapeutics Subcommittee 2 (ET)
Project Start
1979-09-01
Project End
1994-04-30
Budget Start
1989-05-01
Budget End
1990-04-30
Support Year
11
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Barbara Ann Karmanos Cancer Institute
Department
Type
DUNS #
City
Detroit
State
MI
Country
United States
Zip Code
48201
Miller, B E; Matherly, L H; Lehotan, M et al. (1996) Rates of development of methotrexate resistance in heterogeneous mouse mammary tumor cell cultures. J Exp Ther Oncol 1:30-8
Miller, B E; Miller, F R; Machemer, T et al. (1993) Melphalan sensitivity as a function of progressive metastatic growth in two subpopulations of a mouse mammary tumour. Br J Cancer 68:18-25
Heppner, G H (1993) Cancer cell societies and tumor progression. Stem Cells 11:199-203
Miller, B E; Machemer, T; Lehotan, M et al. (1991) Tumor subpopulation interactions affecting melphalan sensitivity in palpable mouse mammary tumors. Cancer Res 51:4378-87
Aslakson, C J; McEachern, D; Conaway, D H et al. (1991) Inhibition of lung colonization at two different steps in the metastatic sequence. Clin Exp Metastasis 9:139-50
Aslakson, C J; Rak, J W; Miller, B E et al. (1991) Differential influence of organ site on three subpopulations of a single mouse mammary tumor at two distinct steps in metastasis. Int J Cancer 47:466-72
Welch, D R; Bisi, J E; Miller, B E et al. (1991) Characterization of a highly invasive and spontaneously metastatic human malignant melanoma cell line. Int J Cancer 47:227-37
Heppner, G H (1991) Cell-to-cell interaction in regulating diversity of neoplasms. Semin Cancer Biol 2:97-103
Miller, F R; McEachern, D; Miller, B E (1990) Efficiency of communication between tumour cells in collagen gel cultures. Br J Cancer 62:360-3
Miller, F R; Heppner, G H (1990) Cellular interactions in metastasis. Cancer Metastasis Rev 9:21-34

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