From Tumor to Bone: Growth Factor Receptors as Key Players in Cancer Metastasis DOI Creative Commons

Khalid S. Mohammad,

Shahid Akhtar Akhund

Frontiers in Bioscience-Landmark, Год журнала: 2024, Номер 29(5)

Опубликована: Май 13, 2024

This review article explores the intricate correlation between growth factors and bone metastases, which play a crucial role in development of several types malignancies, namely breast, prostate, lung, renal cancers. The focal point our discussion is on receptors for factors, including Epidermal Growth Factor Receptor (EGFR), Transforming Factor-β (TGFβ), Vascular Endothelial (VEGFR), Fibroblast (FGFR). These receptors, are essential cellular activities growth, differentiation, survival, have important involvement spread cancer interactions tumors environment. We discuss underlying mechanisms with specific emphasis interaction factor microenvironment. EGFR signaling specifically enhances process osteoclast formation osteolytic lesions, especially breast lung malignancies. TGFβ both osteoblastic metastases by releasing TGFβ, attracts cells promotes remodeling. element prostate to bones. functions FGFR VEGFR processes tumor angiogenesis, respectively, highlight complex diverse nature these interactions. emphasizes possibility targeted therapeutics targeting interrupt cycle degradation. Therapeutic approaches include focusing VEGF/VEGFR, EGF/EGFR, FGF/FGFR, TGFβ/TGFβR pathways. variety compounds, such as small molecule inhibitors monoclonal antibodies, shown potential interfere tumor-induced alterations bone. text discusses clinical trials preclinical models, offering insights into effectiveness constraints various treatments. Ultimately, this study provides succinct but thorough summary present knowledge treatment strategies focused metastases. highlights significance comprehending microenvironment where bones, well using therapies enhance results patients advancement treating hinges treatments that target relationships malignancies

Язык: Английский

Regulatory Role of the Adipose Microenvironment on Ovarian Cancer Progression DOI Open Access
Hussein Chehade, Roslyn Tedja,

Harry Ramos

и другие.

Cancers, Год журнала: 2022, Номер 14(9), С. 2267 - 2267

Опубликована: Май 1, 2022

The tumor microenvironment of ovarian cancer is the peritoneal cavity wherein adipose tissue a major component. role in support progression has been elucidated several studies from past decades. adipocytes, particular, are source factors, which regulate all facets such as acquisition chemoresistance, enhanced metastatic potential, and metabolic reprogramming. In this review, we summarize relevant studies, highlight adipocytes offer insights into unanswered questions possible future directions research.

Язык: Английский

Процитировано

15

Selective Effects of Cold Atmospheric Plasma on Bone Sarcoma Cells and Human Osteoblasts DOI Creative Commons
Andreas Nitsch, Konrad F. Sieb, Sara Qarqash

и другие.

Biomedicines, Год журнала: 2023, Номер 11(2), С. 601 - 601

Опубликована: Фев. 17, 2023

The use of cold atmospheric plasma (CAP) in oncology has been intensively investigated over the past 15 years as it inhibits growth many tumor cells. It is known that reactive oxidative species (ROS) produced CAP are responsible for this effect. However, to translate into medical practice, essential know how treatment affects non-malignant Thus, current vitro study deals with effect on human bone cancer cells and osteoblasts. Here, identical regimens were applied malignant their impact was compared.Two different cell types, U2-OS (osteosarcoma) A673 (Ewing's sarcoma), primary osteoblasts (HOB) used. performed clinically approved kINPen MED. After treatment, kinetics a viability assay performed. For detecting apoptosis, caspase-3/7 TUNEL Accumulated ROS measured culture medium intracellular. To investigate influence motility, scratch carried out.The showed strong inhibition Apoptotic processes enhanced Osteoblasts higher potential resistance comparison There no difference motility between benign following treatment.Osteoblasts show better tolerance indicated by less affected compared CAP-treated This points toward selective sarcoma represents further step clinical application CAP.

Язык: Английский

Процитировано

8

Siglec15 facilitates the progression of non-small cell lung cancer and is correlated with spinal metastasis DOI Open Access

Haifeng Liang,

Qing Chen, Zhichao Hu

и другие.

Annals of Translational Medicine, Год журнала: 2022, Номер 10(6), С. 281 - 281

Опубликована: Март 1, 2022

Background: Non-small cell lung cancer (NSCLC) frequently metastasizes to bone, leading poor prognosis. Siglec15 has been identified as a newly discovered immune checkpoint and exists in variety of tumors. However, the expression function NSCLC bone metastasis remains largely unclear. Methods: correlation between clinicopathological factors patients with were analyzed using The Cancer Genome Atlas (TCGA) dataset. Correlation analysis metastasis-related genes was based on Molecular Signatures Database (MSigDB). Western blotting immunohistochemistry applied detect spinal metastasis. Human A549 mouse CMT167 cells transfected siRNA investigate its biological functions proliferation, migration, invasion. immune-related signaling pathways correlations tumor-infiltrating different checkpoints tumor microenvironment (TME) Estimating Relative Subsets RNA Transcripts (CIBERSORT) gene set enrichment (GSEA). To demonstrate cell-mediated T suppression potential mechanism silencing antitumor immunity, we used killing assay vitro high‑throughput sequencing approach. Results: positively associated stage lymph node metastasis, markedly up-regulated Functionally, knockdown inhibited invasion (A549 lines). A total eight kinds found have strong association cases. previously higher high group. Furthermore, an showed that down-regulation could enhance responses CD8+ cells. High‑throughput revealed molecular mechanisms underlying Siglec15-mediated immunosuppression effect Conclusions: may be involved pathogenesis provide new therapeutic target for treatment

Язык: Английский

Процитировано

13

Wnt Signaling in the Development of Bone Metastasis DOI Creative Commons
Noa Ben-Ghedalia-Peled, Razi Vago

Cells, Год журнала: 2022, Номер 11(23), С. 3934 - 3934

Опубликована: Дек. 5, 2022

Wnt signaling occurs through evolutionarily conserved pathways that affect cellular proliferation and fate decisions during development tissue maintenance. Alterations in these highly regulated pathways, however, play pivotal roles various malignancies, promoting cancer initiation, growth metastasis the of drug resistance. The ability cells to metastasize is primary cause mortality. Bone one most frequent sites metastases generally arise from breast, prostate, lung, melanoma or kidney cancer. Upon their arrival bone, can enter a long-term dormancy period, which they be reactivated, but rarely cured. activation bone process was found enhance proliferation, induce epithelial-to-mesenchymal transition, promote modulation extracellular matrix, angiogenesis immune tolerance thrive bone. Due complexity landscape this mineralized tissue, function metastatic progression within not yet fully understood. Therefore, we believe better understanding could improve our disease may constitute fertile ground for potential therapeutics.

Язык: Английский

Процитировано

13

From Tumor to Bone: Growth Factor Receptors as Key Players in Cancer Metastasis DOI Creative Commons

Khalid S. Mohammad,

Shahid Akhtar Akhund

Frontiers in Bioscience-Landmark, Год журнала: 2024, Номер 29(5)

Опубликована: Май 13, 2024

This review article explores the intricate correlation between growth factors and bone metastases, which play a crucial role in development of several types malignancies, namely breast, prostate, lung, renal cancers. The focal point our discussion is on receptors for factors, including Epidermal Growth Factor Receptor (EGFR), Transforming Factor-β (TGFβ), Vascular Endothelial (VEGFR), Fibroblast (FGFR). These receptors, are essential cellular activities growth, differentiation, survival, have important involvement spread cancer interactions tumors environment. We discuss underlying mechanisms with specific emphasis interaction factor microenvironment. EGFR signaling specifically enhances process osteoclast formation osteolytic lesions, especially breast lung malignancies. TGFβ both osteoblastic metastases by releasing TGFβ, attracts cells promotes remodeling. element prostate to bones. functions FGFR VEGFR processes tumor angiogenesis, respectively, highlight complex diverse nature these interactions. emphasizes possibility targeted therapeutics targeting interrupt cycle degradation. Therapeutic approaches include focusing VEGF/VEGFR, EGF/EGFR, FGF/FGFR, TGFβ/TGFβR pathways. variety compounds, such as small molecule inhibitors monoclonal antibodies, shown potential interfere tumor-induced alterations bone. text discusses clinical trials preclinical models, offering insights into effectiveness constraints various treatments. Ultimately, this study provides succinct but thorough summary present knowledge treatment strategies focused metastases. highlights significance comprehending microenvironment where bones, well using therapies enhance results patients advancement treating hinges treatments that target relationships malignancies

Язык: Английский

Процитировано

2