In a study published previously in Breast Cancer Research
, Castro and colleagues [1
] compared the gene expression signatures of epithelial cells isolated by laser capture micro-dissection (LCM) from non-neoplastic breast tissue, pure ductal carcinoma in situ
(DCIS), DCIS associated with invasive breast cancer, and invasive breast cancer. They found that the expression signature of cells derived from DCIS associated with invasive breast cancer was very similar to that of cells of invasive carcinomas, but differed substantially from cells of pure DCIS.
The observation by Castro and colleagues that cells derived from DCIS associated with invasive cancers show many similarities at the level of gene expression with cells derived from invasive cancers [1
] are consistent with the results of prior studies in which the expression signatures of DCIS and invasive cancers were compared. In those studies, very few genes were found to be differentially expressed in DCIS and invasive breast cancers, particularly those of similar grade, and these studies were unable to define signatures that distinguished between DCIS and invasive cancer [2
]. The results of these prior studies suggest that the most dramatic changes in gene expression occur during the transition from normal epithelium to DCIS rather than in the transition from DCIS to invasive breast cancer. The finding of Castro and colleagues that pure DCIS and DCIS associated with invasive cancer showed a substantial number of differentially expressed genes is of interest and appears to be at odds with this concept. However, these results must be interpreted with caution since only five cases of pure DCIS were studied. Furthermore, these five cases of pure DCIS consisted of a relatively homogenous group of primarily large lesions with high grade nuclei and HER2 overexpression that were compared to a more heterogenous group of DCIS associated with invasive cancer [1
Castro and colleagues propose two possible explanations for the observation that neoplastic cells of DCIS show considerable molecular overlap with cells of invasive breast cancer [1
]. The first possible explanation is that only a small number of genes is associated with the progression of DCIS to invasive breast cancer. The second explanation proposed is that the major molecular alterations associated with invasion are manifested before there is morphologic evidence of invasion at the level of the light microscope. Both of these explanations focus on alterations in the neoplastic epithelial cells as the key determinants of the transition from in situ
to invasive breast cancer. An alternative, albeit not mutually exclusive, explanation is that the progression of DCIS to invasive breast cancer is strongly dependent upon microenvironmental factors, perhaps even more so than on genetic or molecular changes in the neoplastic epithelial cells themselves. In fact, there is now a growing body of evidence supporting a critical role for the tumor microenvironment in breast cancer progression even in its earliest, pre-invasive stages. Components of the microenvironment that have received particular attention in this regard are myoepithelial cells (MECs) and stromal cells (that is, fibroblasts and myofibroblasts).
MECs surround mammary ducts and lobular acini and have important roles in normal mammary gland development and physiology [4
]. In addition, MECs have natural tumor suppressor functions, including maintenance of the basement membrane, providing a physical barrier between epithelial cells and the surrounding stroma, and maintenance of epithelial cell polarity. Furthermore, experimental evidence has indicated that MECs produce factors that, through paracrine effects, inhibit tumor growth, invasion and angiogenesis [6
While MECs are retained around ductal-lobular spaces containing DCIS, recent molecular studies have indicated that MECs that surround spaces involved by DCIS differ substantially from normal MECs in several respects [6
]. When compared to normal MECs, DCIS-associated MECs show downregulation of a variety of genes involved in normal functions, including those for oxytocin receptor, laminin and thrombospondin, and upregulation of genes for chemokines that enhance epithelial cell proliferation, migration, invasion and stromal angiogenesis, such as SDF1
. DCIS-associated MECs also show increased levels of enzymes involved in the degradation of extracellular matrix, such as matrix metalloproteinases [7
]. In addition, a recent study utilizing methylation-specific digital karyotyping demonstrated distinct epigenetic changes in DCIS-associated MECs [9
]. Further, the results of several studies have shown that DCIS-associated MECs show immunophenotypic differences from MECs in normal breast tissue. For example, Hilson and colleagues [10
] found that expression of MEC markers such as smooth muscle myosin heavy chain, CD10 and cytokeratin 5/6 was reduced in the MECs surrounding DCIS in over 80% of the cases evaluated when compared with MECs in normal breast tissue. Taken together, these results provide strong evidence that, in many cases of DCIS, the associated MECs are abnormal. These findings raise the possibility that the progression of DCIS to invasive breast cancer may, at least in part, be due to MEC abnormalities that result in a loss of their normal tumor suppressor functions [5
Other factors in the microenvironment may also be important in regulating the transition from DCIS to invasive breast cancer, such as stromal-epithelial interactions. Stromal cells influence growth, differentiation, invasive behavior and polarity of normal breast epithelial cells and breast cancer cells in vitro
and in vivo
]. In addition, stromal alterations similar to those seen in invasive breast cancers are already evident in association with some cases of DCIS and even in some benign lesions such as radial scars. These include stromal angiogenesis, increased stromal cell expression of mRNAs for various extracellular matrix components, and increased stromal cell expression of proteases and cytokines [12
The molecular determinants of the transition from in situ
to invasive carcinoma in the breast remain to be more clearly elucidated. One approach to address this issue is that used in the study of Castro and colleagues, that is, to utilize LCM to isolate 'pure' populations of epithelial cells and to evaluate molecular alterations in these cells [1
]. However, it should be noted that even when LCM is used, it is not possible to reliably separate epithelial cells from MECs and differences in gene expression between groups (particularly between non-neoplastic breast tissue and DCIS) could well reflect differences in expression of MEC-associated genes rather than epithelial cell-associated genes. Moreover, focusing on changes in the epithelial cells, while important, is tantamount to viewing only one side of a coin. Studies addressing this important question should not ignore the other side of the coin, that is, the potentially important role of the microenvironment in regulating the progression of DCIS to invasive breast cancer.