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      Correlation of RANK and RANKL with mammographic density in primary breast cancer patients

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          Abstract

          Purpose

          The receptor activator of nuclear factor kappa B (RANK) and its ligand (RANKL) have been shown to promote proliferation of the breast and breast carcinogenesis. The objective of this analysis was to investigate whether tumor-specific RANK and RANKL expression in patients with primary breast cancer is associated with high percentage mammographic density (PMD), which is a known breast cancer risk factor.

          Methods

          Immunohistochemical staining of RANK and RANKL was performed in tissue microarrays (TMAs) from primary breast cancer samples of the Bavarian Breast Cancer Cases and Controls (BBCC) study. For RANK and RANKL expression, histochemical scores (H scores) with a cut-off value of > 0 vs 0 were established. PMD was measured in the contralateral, non-diseased breast. Linear regression models with PMD as outcome were calculated using common predictors of PMD (age at breast cancer diagnosis, body mass index (BMI) and parity) and RANK and RANKL H scores. Additionally, Spearman rank correlations (ρ) between PMD and RANK and RANKL H score were performed.

          Results

          In the final cohort of 412 patients, breast cancer-specific RANK and RANKL expression was not associated with PMD ( P = 0.68). There was no correlation between PMD and RANK H score (Spearman’s ρ = 0.01, P = 0.87) or RANKL H score (Spearman’s ρ = 0.04, P = 0.41). RANK expression was highest in triple-negative tumors, followed by HER2-positive, luminal B-like and luminal A-like tumors, while no subtype-specific expression of RANKL was found.

          Conclusion

          Results do not provide evidence for an association of RANK and RANKL expression in primary breast cancer with PMD.

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          Most cited references48

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          RANKL biology: bone metabolism, the immune system, and beyond

          Receptor activator of NF-κB (RANK) ligand (RANKL) induces the differentiation of monocyte/macrophage–lineage cells into the bone–resorbing cells called osteoclasts. Because abnormalities in RANKL, its signaling receptor RANK, or decoy receptor osteoprotegerin (OPG) lead to bone diseases such as osteopetrosis, the RANKL/RANK/OPG system is essential for bone resorption. RANKL was first discovered as a T cell-derived activator of dendritic cells (DCs) and has many functions in the immune system, including organogenesis, cellular development. The essentiality of RANKL in the bone and the immune systems lies at the root of the field of “osteoimmunology.” Furthermore, this cytokine functions beyond the domains of bone metabolism and the immune system, e.g., mammary gland and hair follicle formation, body temperature regulation, muscle metabolism, and tumor development. In this review, we will summarize the current understanding of the functions of the RANKL/RANK/OPG system in biological processes.
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            Mammographic density. Potential mechanisms of breast cancer risk associated with mammographic density: hypotheses based on epidemiological evidence

            There is now extensive evidence that mammographic density is an independent risk factor for breast cancer that is associated with large relative and attributable risks for the disease. The epidemiology of mammographic density, including the influences of age, parity and menopause, is consistent with it being a marker of susceptibility to breast cancer, in a manner similar to the concept of 'breast tissue age' described by the Pike model. Mammographic density reflects variations in the tissue composition of the breast. It is associated positively with collagen and epithelial and nonepithelial cells, and negatively with fat. Mammographic density is influenced by some hormones and growth factors as well as by several hormonal interventions. It is also associated with urinary levels of a mutagen. Twin studies have shown that most of the variation in mammographic density is accounted for by genetic factors. The hypothesis that we have developed from these observations postulates that the combined effects of cell proliferation (mitogenesis) and genetic damage to proliferating cells by mutagens (mutagenesis) may underlie the increased risk for breast cancer associated with extensive mammographic density. There is clearly a need for improved understanding of the specific factors that are involved in these processes and of the role played by the several breast tissue components that contribute to density. In particular, identification of the genes that are responsible for most of the variance in percentage density (and of their biological functions) is likely to provide insights into the biology of the breast, and may identify potential targets for preventative strategies in breast cancer.
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              RANK ligand mediates progestin-induced mammary epithelial proliferation and carcinogenesis.

              RANK ligand (RANKL), a TNF-related molecule, is essential for osteoclast formation, function and survival through interaction with its receptor RANK. Mammary glands of RANK- and RANKL-deficient mice develop normally during sexual maturation, but fail to form lobuloalveolar structures during pregnancy because of defective proliferation and increased apoptosis of mammary epithelium. It has been shown that RANKL is responsible for the major proliferative response of mouse mammary epithelium to progesterone during mammary lactational morphogenesis, and in mouse models, manipulated to induce activation of the RANK/RANKL pathway in the absence of strict hormonal control, inappropriate mammary proliferation is observed. However, there is no evidence so far of a functional contribution of RANKL to tumorigenesis. Here we show that RANK and RANKL are expressed within normal, pre-malignant and neoplastic mammary epithelium, and using complementary gain-of-function (mouse mammary tumour virus (MMTV)-RANK transgenic mice) and loss-of function (pharmacological inhibition of RANKL) approaches, define a direct contribution of this pathway in mammary tumorigenesis. Accelerated pre-neoplasias and increased mammary tumour formation were observed in MMTV-RANK transgenic mice after multiparity or treatment with carcinogen and hormone (progesterone). Reciprocally, selective pharmacological inhibition of RANKL attenuated mammary tumour development not only in hormone- and carcinogen-treated MMTV-RANK and wild-type mice, but also in the MMTV-neu transgenic spontaneous tumour model. The reduction in tumorigenesis upon RANKL inhibition was preceded by a reduction in pre-neoplasias as well as rapid and sustained reductions in hormone- and carcinogen-induced mammary epithelial proliferation and cyclin D1 levels. Collectively, our results indicate that RANKL inhibition is acting directly on hormone-induced mammary epithelium at early stages in tumorigenesis, and the permissive contribution of progesterone to increased mammary cancer incidence is due to RANKL-dependent proliferative changes in the mammary epithelium. The current study highlights a potential role for RANKL inhibition in the management of proliferative breast disease.
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                Author and article information

                Contributors
                peter.fasching@fau.de
                Journal
                Arch Gynecol Obstet
                Arch Gynecol Obstet
                Archives of Gynecology and Obstetrics
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0932-0067
                1432-0711
                5 June 2024
                5 June 2024
                2024
                : 310
                : 2
                : 1223-1233
                Affiliations
                [1 ]GRID grid.5330.5, ISNI 0000 0001 2107 3311, Department of Gynecology and Obstetrics, Comprehensive Cancer Center Erlangen-EMN (CCC ER-EMN), , Erlangen University Hospital, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), ; 91054 Erlangen, Germany
                [2 ]Bavarian Cancer Research Center (BZKF), Erlangen, Germany
                [3 ]GRID grid.5330.5, ISNI 0000 0001 2107 3311, Biostatistics Unit, Department of Gynecology and Obstetrics, Comprehensive Cancer Center Erlangen-EMN (CCC ER-EMN), , Erlangen University Hospital, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), ; 91054 Erlangen, Germany
                [4 ]GRID grid.5330.5, ISNI 0000 0001 2107 3311, Institute of Diagnostic Radiology, Comprehensive Cancer Center Erlangen-EMN (CCC ER-EMN), , Erlangen University Hospital, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), ; 91054 Erlangen, Germany
                [5 ]GRID grid.5330.5, ISNI 0000 0001 2107 3311, Institute of Pathology, Comprehensive Cancer Center Erlangen-EMN (CCC ER-EMN), , Erlangen University Hospital, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), ; 91054 Erlangen, Germany
                [6 ]Immunology in Cancer and Infection Laboratory, QIMR Berghofer Medical Research Institute, ( https://ror.org/004y8wk30) Brisbane, QLD 4702 Australia
                [7 ]Hematology and Oncology Research, Amgen, Inc, ( https://ror.org/03g03ge92) Seattle, WA 98119 USA
                [8 ]GRID grid.42505.36, ISNI 0000 0001 2156 6853, Department of Pathology, Norris Comprehensive Cancer Center, , Keck School of Medicine, University of Southern California, ; Los Angeles, CA 90033 USA
                Author information
                http://orcid.org/0009-0007-7280-7697
                http://orcid.org/0000-0003-4885-8471
                Article
                7495
                10.1007/s00404-024-07495-1
                11258178
                38836929
                842d8c85-e408-4f4b-848f-f822a3629cee
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 12 January 2024
                : 24 March 2024
                Funding
                Funded by: Bayerisch-Kalifornisches Hochschulzentrum
                Funded by: FundRef http://dx.doi.org/10.13039/100001006, Breast Cancer Research Foundation;
                Award ID: BCRF-22-132
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100004802, California Breast Cancer Research Program;
                Award ID: BCRP 12IB-0155
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100005972, Deutsche Krebshilfe;
                Funded by: Universitätsklinikum Erlangen (8546)
                Categories
                Gynecologic Oncology
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2024

                Obstetrics & Gynecology
                breast cancer,mammographic density,rank expression,rankl expression,immunohistochemistry

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