Open Access

The more things change ... the more things change: developmental plasticity of tumor-initiating mammary epithelial cells

Breast Cancer Research201012:101

https://doi.org/10.1186/bcr2459

Published: 18 January 2010

Abstract

In our haste to find and eliminate breast cancer stem cells, it appears as though we may have missed something. Contrary to current thought, a recent paper by Meyer and colleagues demonstrates developmental plasticity of breast cancer cells with respect to the CD24 cell surface marker, such that CD44pos; CD24pos and CD44pos; CD24low/- cells are able to give rise to one another in an activin/nodal-dependent manner, and that cells derived from single cells of either phenotype are capable of forming tumors as xenografts. If confirmed clinically, these data imply that simply targeting the CD44pos; CD24low/- breast cancer stem cell for breast cancer treatment may be destined to fail unless this plasticity is taken into account and prevented.

Change - the one thing you can count on ...

A recent paper by Meyer and colleagues reminds us of this statement, and suggests we may have forgotten something in our rush to exploit the first set of breast cancer stem cell markers identified [1]. Namely, a full analysis of the developmental and tumor-initiating potential of the CD44pos; CD24pos breast cancer cell.

In 2003, two cell surface markers - CD44high and CD24low/- - were associated with breast cancer stem cells [2]. In xenograft transplantation studies, this cell population regenerated tumors at high frequency whereas other cell populations were depleted for this function. Subsequent work in breast cancer cell lines showed that CD44high; CD24low/- cells were present in culture, and were also tumorigenic upon transplantation, with CD24 positivity being associated with decreased invasiveness (for example [3, 4]). Naturally, this work set off a flurry of activity to characterize the CD44high; CD24low/- population molecularly relative to other populations present in tumors [58], and to evaluate their response to treatment (for example [9, 10]).

In the wake of this flurry of activity, it appears we may have forgotten something - to determine the full developmental and tumor-initiating potential of the CD44pos; CD24pos cell. The recent paper by Meyer and colleagues confirms that CD44pos; CD24low/- cells in a number of cell lines can give rise to CD44pos; CD24pos cells, and can yield total populations characteristic of the parental line [1]. This finding is not surprising, and in fact is as expected for a cancer stem cell. Using flow cytometry and single cell culture, however, these authors went on to show that the converse can also occur - CD44pos; CD24poscells can give rise to their CD44pos; CD24low/- counterparts, and are subsequently also capable of initiating tumors as xenografts with high efficiency. Further, their paper shows that the developmental potential for either CD44pos cell population to regenerate the other was dependent on activin/nodal signaling.

While the analysis was limited to established cell lines, what these data imply is that the status of CD24 is dynamically regulated in a developmental context, and suggests that the CD24 status may ultimately be immaterial as to whether or not the CD44pos population is capable of initiating tumors. In addition, these data also imply that current efforts by many groups to develop agents that specifically target the CD44high; CD24low/- population may be destined to fail unless activin/nodal signaling is also prevented.

Aside from the potential implications on translational research, if confirmed clinically, these results beg the question of why we tend to consider mammary tumor-initiating cells as static entities given the fact that the plasticity of normal mammary epithelial cells is, in some circles, the stuff of legends [11].

In the normal gland, plasticity comes in a couple of different forms. First, cellular plasticity - the character of a given cell can change dramatically over the course of gland development (for example, virgin ducts versus pregnancy, or lactation versus involution), and in response to treatment with a bioactive agent (for example, hormones, growth factors). Similarly, there is developmental plasticity - the observation that subsets of mammary epithelial cells retain the ability to give rise to multiple cell types at defined phases of development, although they do not express this ability until needed.

As an example of cellular plasticity, cells already present within the duct of a virgin mouse (and probably of human) in early pregnancy are induced to proliferate and ultimately give rise to alveolar structures capable of producing copious amounts of milk. At least some of these cells can be parity identified after the fact using elegant genetic tagging methods sensitive to at least some degree of alveolar differentiation. Transplantation of these tagged populations suggests that a subset of differentiated alveolar epithelial cells survive the involution process after weaning and retain a high degree of regenerative and multilineage differentiation capacity upon transplantation [12, 13].

With respect to developmental plasticity, we know that regenerative stem cells are present throughout the mature mammary gland in the virgin animal. Small fragments of duct derived from any portion of the gland are capable of regenerating a functional mammary gland when transplanted into a mammary fat pad lacking its endogenous epithelium [14, 15]. If a fragment of duct is transplanted into an intact mammary fat pad already containing epithelium, however, it does not regenerate. Further, actively growing terminal end buds in the mammary gland, which by definition contain regenerative stem cells, do not run into each other and, in fact, are regularly spaced from one another throughout the mammary gland [14].

The inference is that regenerative stem cells resident in the mature duct are not generally actively engaged in stem cell behaviors, and are strongly growth-inhibited by the presence of neighboring normal mammary epithelium. The behavior of regenerative stem cells is thus entirely dependent on the environment in which it finds itself. Further, there is high probability that gene expression in an actively regenerating stem cell is probably quite different from gene expression in a quiescent stem cell.

If normal mammary epithelial cells are plastic, why should we not expect malignant epithelium to share this characteristic?

We are clearly in desperate need of new, rigorously validated, markers of normal and malignant stem cells. Perhaps most importantly, however, we need to ensure that newly emerging therapeutics intended to target tumor-initiating cancer stem cells are evaluated carefully for their ability to eliminate all sources of such cells completely, lest they find a way to express the developmental plasticity with which they appear to be endowed.

Change - count on it.

Declarations

Authors’ Affiliations

(1)
Lester and Sue Smith Breast Center, Department of Molecular and Cellular Biology, and Department of Radiology, One Baylor Plaza

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Copyright

© BioMed Central Ltd 2010

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