Method Article

An In Vitro Dormancy Model of Estrogen-sensitive Breast Cancer in the Bone Marrow: A Tool for Molecular Mechanism Studies and Hypothesis Generation

DOI:

10.3791/52672

June 30th, 2015

In This Article

Summary

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We developed an in vitro model of dormancy in the bone marrow for estrogen-sensitive breast cancer cells. The goal of this protocol is to demonstrate use of the model for the study of the molecular and cellular biology of dormancy and for generation of hypotheses for subsequent testing in vivo.

Abstract

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The study of breast cancer dormancy in the bone marrow is an exceptionally difficult undertaking due to the complexity of the interactions of dormant cells with their microenvironment, their rarity and the overwhelming excess of hematopoietic cells. Towards this end, we developed an in vitro 2D clonogenic model of dormancy of estrogen-sensitive breast cancer cells in the bone marrow. The model consists of a few key elements necessary for dormancy. These include 1) the use of estrogen sensitive breast cancer cells, which are the type likely to remain dormant for extended periods, 2) incubation of cells at clonogenic density, where the structural interaction of each cell is primarily with the substratum, 3) fibronectin, a key structural element of the marrow and 4) FGF-2, a growth factor abundantly synthesized by bone marrow stromal cells and heavily deposited in the extracellular matrix. Cells incubated with FGF-2 form dormant clones after 6 days, which consist of 12 or less cells that have a distinct flat appearance, are significantly larger and more spread out than growing cells and have large cytoplasm to nucleus ratios. In contrast, cells incubated without FGF-2 form primarily growing colonies consisting of >30 relatively small cells. Perturbations of the system with antibodies, inhibitors, peptides or nucleic acids on day 3 after incubation can significantly affect various phenotypic and molecular aspects of the dormant cells at 6 days and can be used to assess the roles of membrane-localized or intracellular molecules, factors or signaling pathways on the dormant state or survival of dormant cells. While recognizing the in vitro nature of the assay, it can function as a highly useful tool to glean significant information about the molecular mechanisms necessary for establishment and survival of dormant cells. This data can be used to generate hypotheses to be tested in vivo models.

Introduction

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Breast cancer cells metastasize to the bone marrow before the disease is detectable1, as soon as small tumors develop blood vessels2,3. The metastatic process is rapid but inefficient. Cells enter the new blood vessels rapidly, at millions per day4 but few survive the trip to distant organs5. Nevertheless, some micrometastases survive in the bone and can be found as single cells or small cell clumps in bone marrow aspirates from newly diagnosed patients1. These cells resist adjuvant chemotherapy, which is administered for the very purpose of eliminating them6. This resistance is endowed, substantially, ....

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Protocol

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1. Clonogenic Assay

  1. Prepare a single cell suspensions of estrogen-dependent breast cancer cell lines MCF-7 and T47D cells using the steps outlined below
    1. Aspirate the culture medium (DMEM/10% heat inactivated fetal calf serum/glutamine and pen/strep) from a 10 cm tissue culture dish which is no more than 50% confluent with MCF-7 or T-47D cells. Rinse with PBS. Incubate with trypsin 0.25%/2.21 mM EDTA dissolved in DMEM high glucose at 37 °C for 1-4 min.
    2. Check cells at 1 min intervals under a phase contrast microscope to ensure a single cell distribution. Resuspend the cells with a 2 ml pipette by pipetting up and down several time....

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Results

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Experiments were conducted to recapitulate the assay. The time course of the experiment is shown in Figure 2A. Cells are incubated at clonogenic density on day -1, FGF-2 in fresh medium is added on day 0 and cells are cultured until day 6 when they are stained and colonies are counted. Any perturbations to the system are administered on day 3 in 100 μl volumes at 10x final concentrations desired. Figure 2B demonstrates the typical appearance of growing and dormant colonies. Growing colon.......

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Discussion

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Our model is comprised of several key elements of dormancy in the bone marrow. It consists of estrogen sensitive cells, which are the type likely to remain dormant in the marrow for extended periods10, it consists of fibronectin, a key structural element of the marrow, FGF-2, a growth factor abundantly synthesized by the bone marrow stroma and heavily deposited in the extracellular matrix of the bone marrow31,32 and incubation of cells at clonogenic density where their interactions are primarily wit.......

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Disclosures

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Supported by the Department of Defense Grants DAMD17-01-C-0343 and DAMD17-03-1-0524, the New Jersey State Commission on Cancer Research 02-1140-CCR-E0 and the Ruth Estrin Goldberg Memorial for Cancer Research (RW)

Acknowledgements

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The authors have nothing to disclose.

....

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
MCF-7 cellsATCCHTB-22
T47D cells ATCCHTB-123
BD BioCoat Fibronectin 24 Well Clear Flat Bottom TC-Treated Multiwell PlateCorning354411
BD BioCoat Fibronectin 60 mm Culture DishesCorning354403
BD BioCoat Fibronectin 100 mm Culture DishesCorning354451
BD BioCoat 22x22mm #1 Glass Coverslip with a uniform application of human fibronectinCorning354088
6 Well tissue culture plateCellTreat229106
Dulbecco Modified Eagle Medium High Glucose 10X PowderCorning Life Sciences50-013-PB
Heat Inactivated, Fetal Bovine SerumSerum Source InternationalFB02-500HI
0.25% Trypsin/2.21 mM EDTACorning25-053-CI
Penicillin-Streptomycin Solution, 100XCorning30-002-CI
L-Glutamine, 100x, LiquidCorning25-005-CI
Recombinant Human FGF basicR&D Systems234-FSE-025
Akt Inhibitor (1L6-Hydroxymethyl-chiro-inositol-2-(R)-2-O-methyl-3-O-octadecyl-sn-glycerocarbonate)CalBiochem124005
LY294002 CalBiochem19-142Chenical PI3K inhibitor
C3 transferase CytoskeletonCTO3Inhibits RhoA, RhoB, and RhoC, but not related GTPases such as Cdc42 or Rac1
Y-27632 dihydrochloride Santa Cruz Biotechnology129830-28-2
BODIPY FL-Phallacidin (green) Molecular ProbesB607Fluorochrome for fibrillar actin staining
BODIPY FL-Rhodamine phalloidin (red) Molecular ProbesR415Fluorochrome for fibrillar actin staining
Alexa Fluor 488 Donkey anti-Mouse IgG Antibody, ReadyProbes Reagent Molecular ProbesR37114
ProLong Gold Antifade Mountant with DAPI Molecular ProbesP-36931

References

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  1. Braun, S., et al. Cytokeratin-positive cells in the bone marrow and survival of patients with stage I, II, or III breast cancer. N Engl J Med. 342 (8), 525-533 (2000).
  2. Benoy, I. H., et al.

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Tags

Bone Marrow DormancyFibronectin Coated PlatesFGF 2 TreatmentClonogenic Density CultureColony Formation AssayPI3K Inhibitor TreatmentCrystal Violet StainingDormant Colony Quantification

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