Human breast adipose tissue: characterization of factors that change during tumor progression in human breast cancer
© The Author(s). 2017
Received: 7 October 2016
Accepted: 27 January 2017
Published: 7 February 2017
Adipose microenvironment is involved in signaling pathways that influence breast cancer. We aim to characterize factors that are modified: 1) in tumor and non tumor human breast epithelial cell lines when incubated with conditioned media (CMs) from human breast cancer adipose tissue explants (hATT) or normal breast adipose tissue explants (hATN); 2) in hATN-CMs vs hATT-CMs; 3) in the tumor associated adipocytes vs. non tumor associated adipocytes.
We used hATN or hATT- CMs on tumor and non-tumor breast cancer cell lines. We evaluated changes in versican, CD44, ADAMTS1 and Adipo R1 expression on cell lines or in the different CMs. In addition we evaluated changes in the morphology and expression of these factors in slices of the different adipose tissues. The statistical significance between different experimental conditions was evaluated by one-way ANOVA. Tukey’s post-hoc tests were performed within each individual treatment.
hATT-CMs increase versican, CD44, ADAMTS1 and Adipo R1 expression in breast cancer epithelial cells. Furthermore, hATT-CMs present higher levels of versican expression compared to hATN-CMs. In addition, we observed a loss of effect in cellular migration when we pre-incubated hATT-CMs with chondroitinase ABC, which cleaves GAGs chains bound to the versican core protein, thus losing the ability to bind to CD44. Adipocytes associated with the invasive front are reduced in size compared to adipocytes that are farther away. Also, hATT adipocytes express significantly higher amounts of versican, CD44 and Adipo R1, and significantly lower amounts of adiponectin and perilipin, unlike hATN adipocytes.
We conclude that hATT secrete a different set of proteins compared to hATN. Furthermore, versican, a proteoglycan that is overexpressed in hATT-CMs compared to hATN-CMs, might be involved in the tumorogenic behavior observed in both cell lines employed. In addition, we may conclude that adipocytes from the tumor microenvironment show a less differentiated state than adipocytes from normal microenvironment. This would indicate a loss of normal functions in mature adipocytes (such as energy storage), in support of others that might favor tumor growth.
KeywordsHuman breast adipose tissue Breast epithelial cells Breast cancer Epithelial-stromal interactions
In addition to epigenetic and genetic changes that occur within epithelial cells, research in the last few years has shown that tumor progression also depends on the dialog between tumor epithelial cells and surrounding stromal cells . Among the different cell types that surround breast tumor epithelial cells, the most abundant are those that compose breast adipose tissue, mainly mature adipocytes, preadipocytes and adipose tissue derived stem cells (ASC). Adipose tissue is a bioactive endocrine organ [2, 3] that secretes soluble factors and contributes significantly to the composition of the extracellular matrix (ECM). Visceral adipose tissue is different from peripheral adipose tissue since it produces a set of unique cytokines and growth factors .
The importance of stromal adipocytes during the development of the normal mammary gland has been recently demonstrated . In addition, in the past few years several groups have demonstrated the importance of the interaction that is established between tumor cells and stromal adipocytes within the invasive front [6, 7]. Cells seem to be able to modify adipocyte phenotype, which in turn, would stimulate tumor aggressive behavior and local invasion . The involvement of factors such as leptin, adiponectin, COLVI, IL-6, HGF and VEGF has been suggested, although there is still a lack of results in human tissues that might confirm their role as well as the potential involvement of new components. Recent studies have demonstrated that growth factors and cytokines secreted by adipose tissue have a significant impact on the progression of several diseases, including breast cancer [3, 8–12]. Statistics show that breast cancer has one of the highest mortality rates around the world. For women in Argentina it is the primary cause of death by cancer (20.1/100,000 women, National Cancer Institute, Argentina, January 2016). Therefore, from a clinical point of view, it is highly relevant to study the involvement of breast adipose tissue in breast cancer development. In particular, it would be relevant to characterize factors secreted by these adipose cells that could modify several aspects of normal and tumor breast epithelial cell lines.
In this study, we focused on ECM proteins, adipokines and their receptors. Versican, a chondroitin sulphate proteoglycan is involved in intracellular signaling and in connecting the cell with the ECM. Increased levels of this proteoglycan have been found in some tumors [13, 14], suggesting that an increase in versican might contribute to tumor progression. Several works have shown that versican seems to be involved in diverse cell functions such as adhesion, migration and proliferation .
CD44, which is a transmembrane glycoprotein that belongs to the family of cell adhesion molecules (CAMs), regulates cell-cell and cell-matrix interactions. Therefore, it plays a key role in cell adhesion and migration. It is also a marker for stem cells in several cell types including epithelial cells and adipocytes [16, 17]. Some works have associated increased levels of CD44 with poor prognosis in cancer development [18, 19].
During the phase of tumor progression, degradation of different local components of the ECM, followed by de novo production of matrix proteins, seem to be fundamental prerequisites for metastatic development. ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) in particular are a group of proteases capable of proteoglycan cleavage and ECM degradation. Some works have described the differential expression of ADAMTS in breast cancer, observing a deregulation of ADAMTS .
Adiponectin and leptin are the two main adipokines secreted by adipocytes. Their role on breast cancer has been extensively studied. Most research show that leptin and adiponectin have opposite effects on cancer development, being leptin pro-tumorigenic and pro-angiogenic [21–23]. However results about these adipokines and their receptors (Adipo R1, Adipo R2 and ObR) have sometimes been contradictory and thus not conclusive .
Models used to study the dialogue between adipose tissue and breast cancer include preadipocyte immortalized cell lines, animal models and 3D culture systems. We have recently shown that conditioned media (CMs) from human breast cancer adipose tissue explants (hATT) regulate proliferation, adhesion and migration of breast cancer epithelial cell lines, as opposed to CMs from normal breast adipose tissue explants (hATN) . In the present work we aim to characterize factors that are modified in tumor and non tumor human breast epithelial cell lines when incubated with hATT- or hATN-CMs, and are possibly involved in the regulation of cell proliferation, adhesion and migration. Specifically, we evaluated changes in the expression of versican, CD44, ADAMTS1, and Adipo R1. In addition, we evaluated the levels of versican and ADAMTS1 in hATN-CMs vs their expression in hATT-CMs. Previously, we have shown that hATT-CMs increase cell migration. In the present work, we found that this effect is lost when hATT-CMs are pre-treated with Chondroitinase ABC. Finally, we observed changes in the phenotype of the tumor associated adipocytes compared to non tumor associated adipocytes; and evaluated by means of immunohistochemistry the expression of versican, adiponectin, AdipoR1, CD44 and perilipin (a marker for mature differentiated adipocytes)  in hATT and hATN.
The identification of these factors, both in adipose tissue and epithelial cells, and the study of their possible involvement in the regulation of tumor progression, might help develop new strategies to prevent and/or treat breast cancer.
Reagents were purchased from Sigma Chemical Co (St. Louis, MO, USA), tissue culture flasks, dishes, and multi-well plates were from Falcon Orange Scientific (Graignette Business Park, Belgium), culture media and supplements for both tissue and cell lines were from Gibco BRL (Carlsbad, CA, USA).
Sample collection and handling
For the experiments we used fragments of adipose tissue from both tumoral (hATT, n = 22) and normal breasts (hATN, n = 16). These fragments were embedded in paraffin. hATT tissue samples were obtained from estrogen and/or progesterone receptor positive, stage GH2, infiltrating ductal carcinomas. None of the patients had received chemotherapy or radiotherapy treatment. hATN tissue samples were obtained from plastic surgeries performed for aesthetic reasons (breast reduction). Al samples were processed within 2 h under a sterile laminar flow hood. At arrival, tissue was transferred to a Petri dish and was extensively washed with 50 ml ice PBS supplemented with gentamicin (50 μg/ml). Thereafter, tissues were transferred to a 50 ml centrifuge tube containing 45 ml phosphate buffer saline solution (PBS) at 37 °C and gently shaken for 5 min and centrifuged for 1 min at 277 x g at RT to remove red blood cells and debris. Tissue was then removed from the tube and weighed. hATT or hATN tissue was placed in a culture flask with M199 culture medium (Invitrogen™) (1 g tissue/10 ml M199) supplemented with gentamicin (50 μg/ml) and incubated for 1 h at 37 °C in 5% CO2. After this time, medium was removed and replaced with fresh medium. After 24 h CM was collected, centrifuged, filtrated and aliquoted into 1 ml fractions and immediately stored at -80C, until its use. M199 medium was used as Control-CM. All patients gave their written consent. Samples (tumor and normal) were collected following the approval of the Ethics Committee of the IBYME .
Culture of tumor and non-tumor breast epithelial cell lines
Immortalized epithelial cell lines from human tumor (MCF-7 or IBH7) and non tumor (MCF10-A and HBL100) breasts were used. MCF-7, MCF-10A and HBL100 were obtained from the American Type Culture Collection (ATCC, Rockville, MD, USA), whereas IBH-7 is a line immortalized from a primary breast tumor by the laboratory of Dr. Isabel Luthy [26, 27]. MCF10-A cell line cultures were grown in DMEM-F12 medium supplemented with 10% bovine fetal serum (BFS), insulin (2 μg/ml), cortisol (0.5 μg/ml) and EGF (20 ng/ml) and antibiotics; while the remaining cell line cultures were grown in DMEM-F12 supplemented with 10% BFS and insulin (2 μg/ml), and antibiotics. All cultures were kept at 37 °C in a 5% CO2 atm.
Breast epithelial cell proliferation assay
Tumor (3x103 MCF-7 or IBH-7 cells/well) and non-tumor (5x103 MCF-10A or HBL100 cells/well) human breast epithelial cell lines were incubated on 96-well plates with complete DMEM-F12 for 24 h. Then, the four cell lines were treated with hATN-, hATT- or control-CMs for an additional 48 h, at 50% CM (50% hATN-, hATT- or control-CMs and 50% DMEM-F12 medium) or 75% CM (75% hATN-, hATT- or control-CMs and 25% DMEM-F12 medium). The number of viable cells was determined by a commercial colorimetric kit (Cell titer 96 AQueous One Solution Cell Proliferation Assay, MTS). Results are expressed as percentage of color intensity and normalized to cells grown in control-CMs.
Preparation of cell lysates from breast epithelial cells after incubation with hATN-CMs or hATT-CMs
MCF-10A, HBL100, MCF-7 and IBH-7 cells were seeded in six-well plates in DMEM-F12 complete medium. When cells reached 75–80% confluence, the medium was aspirated and cells were washed twice with PBS. Then, cells were incubated at 37 °C for 24 h either with hATT-, hATN-, or control-CMs (50% CM, 50% DMEM-F12). Cells were lysed with Ripa buffer, pelleted by centrifugation at 4 °C and stored at −80 °C.
Tumor (MCF-7 or IBH-7) and non-tumor (MCF-10A and HBL100) were seeded on Lab Tek Chamber Slide system until they reached 50–60% confluence. They were then incubated with hATT-, hATN-, or control-CMs for 24 h (50% CM, 50% DMEM-F12). An additional control without primary antibody was performed as antibody specificity control. Cells were fixed with formaldehyde, washed, blocked and permeabilized (PBS-BSA 0.2%-Triton X100 0.3% for 30 min). They were then incubated with 100 μl of anti-versican primary antibody (Santa Cruz, USA) at 4 °C. In order to increase specificity, primary antibody unspecific activity was blocked with goat serum. Cells were then washed and incubated with the second antibody conjugated to FITC (Sigma) for 1 h. Finally they were incubated for 10 min with propidium iodide to visualize nuclei. Cell localization (nuclear or cytoplasmic) was visualized, and fluorescence intensity was quantified per cell using ImageJ 1.42q software available at the NIH site (http://rsb.info.nih.gov/ij).
Western blot analysis
In order to evaluate protein expression levels, Western blots were performed. Versican, CD44, ADAMTS1 and Adipo R1 were measured after incubation of the epithelial cell lines with the different CMs obtained. In order to lyse cells, Ripa buffer was used (Tris 10 mM pH 7,5; NaCl 150 mM; sodium vanadate 2 mM; sodium deoxycholate; SDS 0,1%; igepal 1%; protease inhibitors). In addition, versican and ADAMTS1 expression was measured in CMs-hATT and CMs-hATN. Total protein in samples was quantified by Bradford method. Proteins were separated in a SDS-PAGE 10% gel, and electrotransferred to a nitrocellulose membrane (Amersham). The membrane was later blocked with bovine serum albumin (Sigma-Aldrich, 0055 K) and then incubated with the different antibodies ON at 4 °C. The membranes were later washed, and incubated with proper secondary antibodies conjugated to HRP. Antibody complexes were visualized by means of chemiluminescence (ECL; GE Helathcare). Band density was measured by means of SCION ImageTM software (Scion Corporation, Maryland, USA). In the cell extracts, β-actin level in samples was used to determine that equal quantities of proteins were loaded in the gel.. The assay for the CMs-hATT and CMs-hATN was done by loading equal volumes of each CM.
Breast epithelial cell migration assays (“wound-healing”)
The effect of hATN- or hATT-CMs, with or without Chondroitinase ABC, on the motility of tumor breast epithelial cell lines was evaluated by wound-healing assays.
MCF-7 and IBH-7 cells were grown on 96-well plates with complete DMEM-F12 until cells reached 100% confluence. After, cell monolayers were scratched with a 200 μl pipette tip, washed twice with PBS and hATN-, hATT- or control-CMs were added. CMs were pre-treated with Chondroitinase ABC (final concentration 80 mU/ml) (Sigma C2905) or PBS for 1 h at 37 °C. Images at time zero (0 h) were captured to record the initial width of the wounds, and the recovery of the wounded monolayers due to cell migration toward the denuded area was evaluated at 6 h. The images were captured using an inverted phase-contrast microscope (Olympus CKX-41; 4x objective). A quantitative analysis of the wound closure was measured by Java Image J (NIH, Bethesda, MD, USA) software using the freehand selection mode and determined the relative wound closure respect to control of the wounded area after 6 h.
Tissues (hATT and hATN) were fixed in 4% formaldehyde and embedded in paraffin. They were afterwards cut into sections of 3 μm thickness with a microtome, deparaffinized and stained with hematoxylin-eosin (H&E). Images were taken with a Nikon Eclipse E200 Microscope fitted with a digital still camera Micrometric SE Premium (Nikon Corp., Japan) at 100x magnification. Adipocyte area quantification (measuring adipocyte perimeter) in the three tissue types was performed in 8–10 fields of each preparation as mentioned above. In particular, we compared tissues obtained from hATN with two different areas of hATT: adipose tissue attached to the primary tumor; and adipose tissue obtained 2 cm away from the tumor.
Serial cuts were performed on the same tissue samples used for H&E staining. Versican, adiponectin, Adipo R1, CD44, and perilipin expression were studied by means of immunohistochemistry. Briefly, hATT and hATN microtome slides were first deparaffinized, and then a heat-mediated antigen retrieval, endogenous peroxidase blocking and nonspecific tissue blocking were performed. Slides were then incubated with the different primary antibodies at 4 °C, and after that with an anti-rabbit biotinylated secondary IgG antibody. Finally, slides were incubated with peroxidase-conjugated streptavidin. Peroxidase reaction was performed with chromogen 3,3′-diaminobenzidine (DAB) (DAKO LSAB + Kit, HRP). Hematoxylin counter stain was performed. Serial cuts incubated in the absence of primary antibody were used as negative controls. Images were taken with a Nikon Eclipse E200 Microscope fitted with a Micrometric SE Premium (Nikon Corp., Japan) digital still camera at 100x and 400x magnifications. DAB staining quantification in the three tissue types was performed in 8–10 fields of each preparation as mentioned above.
The statistical significance between different experimental conditions was evaluated by one-way ANOVA. Tukey’s post-hoc tests were performed within each individual treatment. The results are presented as mean ± SEM. Results were considered significant at p < 0.05.
hATT-CMs increase proliferation of tumor and non-tumor epithelial cell lines in a dose-dependent manner
These results are in accordance with previous ones by our group , and suggest the presence of soluble factors in hATT-CMs (either absent or present at lower concentrations, in hATN-CMs) that would stimulate the proliferation of both tumor and non-tumor epithelial cells. The characterization of soluble factors in both CMs will help to elucidate this question.
hATT-CMs increase versican expression in breast cancer epithelial cells
Versican proteoglycan can participate in the regulation of cell motility, growth, differentiation and angiogenesis. Its cell location has been described to depend on growth conditions and cell type. Preliminary results had shown presence of versican in the cell lines employed. Nevertheless, we modified the antibody protocol to confirm the specificity of the antibody used to recognize versican (primary antibody unspecific activity was blocked with goat serum).
The increase in the expression of versican was also observed by Western-blot, in cell lysates of MCF-7 and IBH-7 incubated with hATT-CMs compared to the expression found with hATN-CMs and control-CMs (Fig. 2e).
hATT-CMs increase CD44, ADAMTS1 and Adipo R1 expression in breast tumor cancer epithelial cells
We evaluated possible changes in the expression of these proteins in the different cell lines incubated with the CMs (hATT-, hATN- or control-CMs).
ADAMTS1 is a member of a group of peptidases (different from proteases) that are able to cleave proteoglycans and degrade the ECM. Our results indicate an increased expression of the 87 kDa form of ADAMTS1 in MCF-7 and IBH-7 tumor cells incubated with hATT-CMs vs. hATN- or control-CMs (Fig. 3b).
Adipose tissue produces adiponectin, which has been proposed to be involved in breast cancer regulation through its membrane receptors. Our results indicate an increased expression of Adipo R1 in MCF-7 and IBH-7 tumor cells incubated with hATT-CMs vs. hATN- or control-CMs (Fig. 3b).
No significant differences were found with any treatment in non-tumor cells MCF-10A and HBL100.
hATT-CMs present increased versican expression, and no significant changes in ADAMTS1 expression, compared to hATN-CMs
We evaluated the expression of the proteoglycan versican and metalloproteinase ADAMTS1 in hATT- and hATN-CMs. Previous research has described the differential expression of ADAMTS1 in breast cancer and a deregulation of ADAMTS1 in this cancer type.
Chondroitinase ABC treatment of hATT-CMs eliminates their effect on cell migration of breast cancer epithelial cells
Adipocytes associated with the invasive front are reduced in size compared to adipocytes that are farther away
hATT adipocytes showed significantly higher expression of versican, Adipo R1 and CD44, and significantly lower expression of adiponectin and perilipin, unlike hATN adipocytes
Stromal-epithelial interactions mediate the development and progression of breast cancer. Adipocytes are the predominant stromal cell type in breast tissue. We have recently shown that CMs from human adipose tissue explants of breast tumors differentially regulate the proliferation, adhesion and migration of breast cancer epithelial cell lines, compared to CMs from adipose tissue explants of normal breast samples . In the present work we aimed to characterize factors that could be modified in tumor and non-tumor human breast epithelial cell lines, when incubated with hATT- or hATN-CMs, as possible candidate factors responsible of the observed biological effects. Specifically, we evaluated changes in the expression of versican, CD44, ADAMTS1 and Adipo R1. In addition, we evaluated the expression of versican and ADAMTS1 in hATN-CMs vs their expression in hATT-CMs. Finally, we observed changes in the phenotype of tumor-associated adipocytes compared to non tumor associated adipocytes; and evaluated with immunohistochemistry versican, adiponectin, Adipo R1, CD44, and perilipin expression in hATT and hATN slides. hATT-CMs significantly increased (in a dose dependent manner) tumor and non tumor epithelial cell proliferation. These results confirm previous observations already reported by our group, suggesting that soluble factors present in hATT-CMs stimulate breast epithelial cell proliferation in a dose-dependent manner, whether cells are tumor or not. These factors would appear not to be present (or present at lower concentrations) in hATN-CMs.
The identification of factors that might be modified in tumor and non-tumor breast epithelial cell lines when in contact with products secreted by adipose tissue from breast cancer samples, could allow studying the mechanisms by which adipose tissue might regulate tumor growth and progression. Previous works described versican as a component of the ECM; and it has been proposed that from this location it would help regulate cellular mechanisms such as proliferation, migration and angiogenesis. Nevertheless, recent experiments have also found an intracellular localization of versican, which implies new action mechanisms for this proteoglycan [28–30]. In accordance with these last reports, we observed that versican presents both a nuclear and a cytoplasmic distribution, although its nuclear values were higher. In addition, when tumor cells were incubated with hATT-CMs we observed an increase in total cell fluorescence compared to hATN- and control-CMs. Considering the nature of previous results, we propose that the observed increase in fluorescence intensity could be related to an increase in versican expression. We confirmed the observed increase of expression with a Western blot. Since versican presents 4 different isoforms, and it has been already seen that these isoforms have different functions , in future works we will analyze if there are changes in the proportion of these different isoforms, in addition to the increase in total expression.
Additionally, our results show that in breast cancer epithelial cells, hATT-CMs increase: 1) membrane glycoprotein CD44 (which plays a key role in cell adhesion as well as in cell migration); 2) metalloproteinase ADAMTS1 (which is capable of proteoglycan cleavage and ECM degradation); 3) adiponectin type 1 receptor (one of adiponectin receptors). In order to mechanistically evaluate the importance of these genes in cell proliferation, adhesion and migration, we will perform a loss- or gain-of-function in future experiments.
The identification of factors involved in the interaction between adipose and breast epithelial tissue could potentially allow us to regulate the expression of one or more of these factors in order to reverse tumor behavior.
Our results showed an increase of versican expression in CMs from hATT compared to CMs from hATN. This could indicate that verisican might be involved in the regulation of cell proliferation, adhesion and migration. To confirm, we performed an additional experiment in which we evaluated cell migration of MCF-7 and IBH-7 incubated with control-, hATN- and hATT-CMs pretreated (or not) with Chondroitinase ABC, an enzyme that degrades versican’s GAG chains. It has been reported that versican interacts with CD44, and this interaction depends on versican’s GAG chains [32, 33]. We found a loss of effect in cell migration values when hATT-CMs were pretreated with Chondroitinase ABC, thus strengthening the view that versican produced by adipocytes is involved at least in part in the biological effects seen in Pistone Creydt et al. .
ADAMTS1 gene is down-regulated in breast carcinomas with respect to non neoplastic mammary tissue . Nevertheless it has been recently demonstrated that ADAMTS1 promotes breast tumor cell migration by regulating the release of semaphorin 3c from the ECM . These apparently contradictory results could be due to the fact that ADAMTS1 presents two distinct active forms, an 87 kDa and a 65 kDa form, which have been describe to present different functions . Although we didn’t find a significant difference in the levels of the 65 kDa form of this metalloproteinase in the hATT-CMs and hATN-CMs, a tendency to be increased in the hATN-CMs was seen. Since the 65 kDa form is mainly detached from the ECM and it has been reported to have anti-angiogenic properties, this could show a way in which a normal adipose microenvironment prevents angiogenesis in distant locations. Nonetheless, more samples need to be assessed to confirm these results. Furthermore, since an increase in ADAMTS1 expression not necessarily correlates with an increase in ADAMTS1 activity, we shall measure the activity of this peptidase in the different CMs and in the lysates of cells treated with the CMs.
In the last few years, several groups have demonstrated the importance of the dialogue that is established in the invasive front between tumor cells and stromal adipocytes [6, 7]. Tumor cells would be able to modify adipocyte phenotype, which in turn would stimulate the tumor’s aggressive behavior and local invasion . We observed that the characteristics of the connective tissue were modified in response to the local invasion of tumor cells. Specifically, adipocytes associated to the tumor’s invasive front showed a reduced size compared to those found farther away (2 cm) and from adipocytes from normal breasts. In addition, we observed a significantly higher expression of versican, CD44 and Adipo R1, and significantly lower expression of adiponectin and perilipin, in hATT adipocytes compared to hATN adipocytes. We believe that the observed overexpression of Adipo R1 in both hATT tissue explants, and MCF-7 and IBH-7 cells incubated with hATT-CMs are an up-regulation compensatory mechanism as a consequence of the decreased levels of adiponectin secreted by peritumoral adipocytes. Serum adiponectin levels have been seen to significantly decrease in breast-cancer patients, while antiproliferative effects of adiponectin, as well as cell cycle inhibition and activation of apoptosis have been verified in most studies . Our results are in line with these previous experiments, since they show that adiponectin levels are decreased in hATT tissue explants. In addition, we observed that perilipin (marker of mature adipocytes) is decreased and CD44 is increased in hATT versus hATN. This would mean that the adipocytes of the tumor microenvironment present a less differentiated state than the adipocytes of the normal microenvironment. This would indicate a loss in normal functions of mature adipocytes, such as energy storage, by others that could be favoring tumor development. These results begin to clarify early phenotypic and genotypic changes that undergo adipocytes that are in direct contact or farther away from the invasive tumor epithelium.
We conclude that versican, a proteoglycan that is overexpressed in hATT-CMs compared to hATN-CMs, might be involved in the tumorogenic behavior observed in both cell lines employed. In addition, we may conclude that adipocytes from the tumor microenvironment show a less differentiated state than adipocytes from normal microenvironment. This would indicate a loss of normal functions in mature adipocytes (such as energy storage), in support of others that might favor tumor growth. The analysis and characterization of the factors that modify their expression, both in adipose tissue as well as epithelial cells, and the study of the involvement of these factors in the regulation of tumor progression, might allow developing new strategies to prevent and/or treat breast cancer.
The authors thank Dr. María Luján Crosbie, Dr. Anabela Ursino, Dr. Santiso Natalia, Dr. Alicia Rita Amato, Dr. Celeste Frascarolli, and Dr. Albertto Gutiérrez from the Churruca-Visca Medical Center, Buenos Aires, Argentina for collecting additional samples of adipose tissue.
This work was partially supported by grants to Dr. Virginia Pistone Creydt: PIP 2011–2013 from CONICET and Subsidio para Investigación Médica 2013–2015 from Lab. Roemmers.; and Honorio Bigand Fundation.
Availability of data and materials
SJF participated in the design of the study, performed part of the experiments and helped draft the manuscript. PAS participated in the design of the study. MPC contributed with part of the biological samples used and drafted the manuscript. FAC contributed with part of the biological samples used and drafted the manuscript. MFS performed part of the experiments and contributed to the discussion of the results. FES performed part of the experiments and contributed to the discussion of the results. CVS performed part of the experiments and contributed to the discussion of the results. CMLP performed part of the experiments and contributed to the discussion of the results. RWC participated in coordinating and drafting the manuscript. JCC conceived the study, and participated in its design and coordination and helped draft the manuscript. VPC conceived the study, performed part of the experiments, and participated in its design and coordination and helped draft the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
All patients gave their written consent. Samples (tumor and normal) were collected following the approval of the Ethics Committee of the IBYME.
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