Molecular Mechanisms of Bone Metastases

A special issue of Biomolecules (ISSN 2218-273X). This special issue belongs to the section "Molecular Medicine".

Deadline for manuscript submissions: closed (31 January 2022) | Viewed by 17118

Special Issue Editors


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Guest Editor
Dipartimento di Scienze Biomediche per la Salute, Università degli Studi di Milano, Milano, Italy
Interests: invasive growth; breast cancer; bone metastasis; signal transduction; protein kinases; growth factor receptors; cytokines; epithelial–mesenchymal transition; tumor microenvironment
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Guest Editor
Laboratory of Experimental Biochemistry & Molecular Biology, IRCCS Istituto Ortopedico Galeazzi, Via Riccardo Galeazzi 4, 20161 Milano, Italia
Interests: breast cancer; bone metastasis; tumor microenvironment; invasive growth; epithelial–mesenchymal transition; autophagy; signal transduction; immunohistochemistry; animal models
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Bone metastasis represents the leading cause of death for some cancers, such as breast, prostate, lung, kidney, and thyroid cancer. Multiple myeloma also prefers to grow and metastasize in the bone marrow. Therefore, bone metastases represent a critical issue in the field of oncology.

The bone-metastatic process is complex; it begins early with the preparation of a pre-metastatic niche by the primary tumor to create a microenvironment which is useful for the establishment and growth of metastatic cells. It then goes through several steps leading to the formation of lesions that result in bone resorption or excessive bone formation. Bone tissue provides a unique environment (low oxygen concentration, mineral content, acidic pH, elevated concentration of calcium) for metastatic cells, creating a fertile ground for growth, so tumor–stroma interaction drives the progression of the lesion. Cancer cells co-opt the bone marrow microenvironment to promote their own survival, growth, and metastatic progression.

Although our knowledge of the biological events involved in metastasis is increasingly clear, much remains to be done to achieve the goal of preventing or blocking bone metastases when they are at an early stage or treating them.

The purpose of this Issue is to take stock of the molecular mechanisms involved in the establishment and evolution of the bone-metastatic process since the understanding of the events involved in its formation is fundamental for developing molecular-target therapies to reduce the negative and destructive impact of metastasis. Studies aimed at the identification of molecules with prognostic value are also of paramount importance for the prevention of bone metastasis development. Original articles and reviews will be considered.

This Special Issue is jointly organized between Biomolecules and Biomedicines. In accordance with the Aims and Scope of these journals, articles showing basic studies in biochemistry, molecular biology, and molecular medicine can be submitted to Biomolecules, whereas articles referring to cancer biology and therapeutics or with more clinical content can be submitted to Biomedicines.

Dr. Paola Bendinelli
Dr. Paola Maroni
Guest Editors

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Keywords

  • Bone metastases
  • Tumor invasion
  • Biomarkers
  • Non-coding RNAs (miRNAs, lncRNAs and circRNAs)
  • Exosomes/extracellular vesicles
  • Circulating tumor cells (CTCs)
  • Tumor microenvironment
  • Metalloproteases
  • Cancer-associated fibroblasts
  • Cytokines
  • Growth factors
  • Protein kinases

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Published Papers (3 papers)

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Research

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9 pages, 3260 KiB  
Article
Impaired Alignment of Bone Matrix Microstructure Associated with Disorganized Osteoblast Arrangement in Malignant Melanoma Metastasis
by Aira Matsugaki, Yumi Kimura, Ryota Watanabe, Fumihito Nakamura, Ryo Takehana and Takayoshi Nakano
Biomolecules 2021, 11(2), 131; https://doi.org/10.3390/biom11020131 - 20 Jan 2021
Cited by 6 | Viewed by 2774
Abstract
Malignant melanoma favors spreading to bone, resulting in a weakened bone with a high fracture risk. Here, we revealed the disorganized alignment of apatite crystals in the bone matrix associated with the homing of cancer cells by developing an artificially controlled ex vivo [...] Read more.
Malignant melanoma favors spreading to bone, resulting in a weakened bone with a high fracture risk. Here, we revealed the disorganized alignment of apatite crystals in the bone matrix associated with the homing of cancer cells by developing an artificially controlled ex vivo melanoma bone metastasis model. The ex vivo metastasis model reflects the progressive melanoma cell activation in vivo, resulting in decreased bone mineral density and expression of MMP1-positive cells. Moreover, less organized intercellular connections were observed in the neighboring osteoblasts in metastasized bone, indicating the abnormal and randomized organization of bone matrix secreted by disconnected osteoblasts. Our study revealed that the deteriorated microstructure associated with disorganized osteoblast arrangement was a determinant of malignant melanoma-related bone dysfunction. Full article
(This article belongs to the Special Issue Molecular Mechanisms of Bone Metastases)
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Review

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23 pages, 8227 KiB  
Review
The Role of TGF-β in Bone Metastases
by Trupti Trivedi, Gabriel M. Pagnotti, Theresa A. Guise and Khalid S. Mohammad
Biomolecules 2021, 11(11), 1643; https://doi.org/10.3390/biom11111643 - 6 Nov 2021
Cited by 40 | Viewed by 5586
Abstract
Complications associated with advanced cancer are a major clinical challenge and, if associated with bone metastases, worsen the prognosis and compromise the survival of the patients. Breast and prostate cancer cells exhibit a high propensity to metastasize to bone. The bone microenvironment is [...] Read more.
Complications associated with advanced cancer are a major clinical challenge and, if associated with bone metastases, worsen the prognosis and compromise the survival of the patients. Breast and prostate cancer cells exhibit a high propensity to metastasize to bone. The bone microenvironment is unique, providing fertile soil for cancer cell propagation, while mineralized bone matrices store potent growth factors and cytokines. Biologically active transforming growth factor β (TGF-β), one of the most abundant growth factors, is released following tumor-induced osteoclastic bone resorption. TGF-β promotes tumor cell secretion of factors that accelerate bone loss and fuel tumor cells to colonize. Thus, TGF-β is critical for driving the feed-forward vicious cycle of tumor growth in bone. Further, TGF-β promotes epithelial-mesenchymal transition (EMT), increasing cell invasiveness, angiogenesis, and metastatic progression. Emerging evidence shows TGF-β suppresses immune responses, enabling opportunistic cancer cells to escape immune checkpoints and promote bone metastases. Blocking TGF-β signaling pathways could disrupt the vicious cycle, revert EMT, and enhance immune response. However, TGF-β’s dual role as both tumor suppressor and enhancer presents a significant challenge in developing therapeutics that target TGF-β signaling. This review presents TGF-β’s role in cancer progression and bone metastases, while highlighting current perspectives on the therapeutic potential of targeting TGF-β pathways. Full article
(This article belongs to the Special Issue Molecular Mechanisms of Bone Metastases)
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18 pages, 1113 KiB  
Review
Mediterranean Diet Food Components as Possible Adjuvant Therapies to Counteract Breast and Prostate Cancer Progression to Bone Metastasis
by Paola Maroni, Paola Bendinelli, Alessandro Fulgenzi and Anita Ferraretto
Biomolecules 2021, 11(9), 1336; https://doi.org/10.3390/biom11091336 - 9 Sep 2021
Cited by 4 | Viewed by 7860
Abstract
Bone metastasis is a serious and often lethal complication of particularly frequent carcinomas, such as breast and prostate cancers, which not only reduces survival but also worsens the patients’ quality of life. Therefore, it is important to find new and/or additional therapeutic possibilities [...] Read more.
Bone metastasis is a serious and often lethal complication of particularly frequent carcinomas, such as breast and prostate cancers, which not only reduces survival but also worsens the patients’ quality of life. Therefore, it is important to find new and/or additional therapeutic possibilities that can counteract the colonization of bone tissue. High adherence to the Mediterranean diet (MD) is effective in the prevention of cancer and improves cancer patients’ health, thus, here, we considered its impact on bone metastasis. We highlighted some molecular events relevant for the development of a metastatic phenotype in cancer cells and the alterations of physiological bone remodeling, which occur during skeleton colonization. We then considered those natural compounds present in MD foods with a recognized role to inhibit or reverse the metastatic process both in in vivo and in vitro systems, and we reported the identified mechanisms of action. The knowledge of this bioactivity by the dietary components of the MD, together with its wide access to all people, could help not only to maintain healthy status but also to improve the quality of life of patients with bone metastases. Full article
(This article belongs to the Special Issue Molecular Mechanisms of Bone Metastases)
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