Increasing evidence reveals the heightened expression of olfactory receptors in tumorous tissues and Olfactory receptors have demonstrated influence over tumor cell proliferation and metastasis, establishing a close relationship with tumor initiation and progression. The potential for precise tumor diagnosis and targeted therapy through therapeutic targeting of olfactory cell proliferation , Tumor development , Tumor metastasis .

GPCRs in Oncology and Immunology Exploiting frequent and specific expression of PRL3 in pediatric solid tumors Published date September 21, 2023 Abstract "Phosphatase of regenerating liver 3 (PRL3) is a specific tumor However, its physiological expression in pediatric embryonal and mesenchymal tumors and its association Among 64 pediatric tumors, PRL3 was most frequently expressed in neuroblastoma (100%), rhabdomyosarcoma PRL3 was expressed in 75% of relapsed tumors and associated with shorter median event-free survival.

P2Y12R activation can promote platelet aggregation and adhesion to cancer cells, promote tumor angiogenesis , and affect the tumor immune microenvironment (TIME) and tumor drug resistance, which is conducive to We explored the role of P2Y12R inhibitors in different tumors and the latest advances by summarizing the basic and clinical studies on the effects of P2Y12R inhibitors on tumors." , Tumor microenvironment Source Contribute to the GPCR News Coming soon Become a Contributor Classified

typical GPCR with a high affinity for adenosine, is widely expressed on immune cells, inhibiting anti-tumor Here, we identify that A2aR is specifically expressed on tumor cells from lung adenocarcinoma (LUAD) patients, closely related to their prognosis and positively correlated with tumor-associated macrophages We hypothesize that blocking A2aR on LUAD cells will inhibit the role of TAMs and control tumor growth Functionally, blocking A2aR significantly suppresses TAMs infiltration and attenuates tumor burden in

< GPCR News < GPCRs in Oncology and Immunology Metabolic crosstalk: Extracellular ATP and the tumor microenvironment signals inside the body, which is necessary for controlling the life activities of all cells, including tumor Its significance extends from intracellular signaling pathways to tumor regression. In the tumor microenvironment (TME), purinergic receptors such as ATP-gated ion channels P2X1-5 and G (e-ATP) , Immunosuppression , Purinergic receptors , Purinergic signaling , Therapeutic potential , Tumor

GPCR News < GPCRs in Oncology and Immunology RGS5 maintaining vascular homeostasis is altered by the tumor VSMCs and pericytes, which is involved in VSMC phenotypic heterogeneity and vascular remodeling in tumors However, its role in normal and tumor vascular remodeling is controversial. Furthermore, tumor-derived RGS5 could be transferred into VSMCs. to pro-inflammation and induces the pro-inflammatory phenotype of VSMCs that is favorable for tumor

receptors are clinically validated GPCR biomarkers for diagnosis and treatment of various neuroendocrine tumors performed immunohistochemistry of paired tissue microarrays containing 1125 cores, representing 43 tumor (ovarian and hepatocellular adenocarcinomas) as a function of their tumor stage. The expression prevalence of both receptors tends to decline with tumor progression. both SST2 and SST3 reemerged in metastases suggesting conserved receptors genetic potential during tumor

GPCRs in Oncology and Immunology G protein-coupled receptor-mediated signaling of immunomodulation in tumor Published date July 31, 2024 Abstract "G protein-coupled receptors (GPCRs) are essential contributors to tumor Here, we discuss the current understanding of the roles of GPCRs and their signaling pathways in tumor This expanded understanding of the role of GPCRs may shed light on the mechanisms underlying tumor progression Qiu, Bin Yu, Mei Ma Tags GPCRs , cancer immune checkpoints , cancer immunotherapy , immune cells , tumor

< GPCRs in Oncology and Immunology Aberrant hormone receptors regulate a wide spectrum of endocrine tumors of diverse GPCRs and their ligands play an important role in the over-function of various endocrine tumours ; AVPR2, D2DR, and SSTR5 in pituitary corticotroph tumours; GLP1R, GIPR, and somatostatin receptors in medullary thyroid carcinoma; and SSTRs, GLP1R, and GIPR in other neuroendocrine tumours. to cortisol-secreting adrenal lesions, but also occurs in tumours of several other organs."

paradoxical roles in both the directed emigration of metastatic, receptor-expressing cancer cells out of the tumor as well as immigration of tumor infiltrating immune cells that culminate in a tumor unique immune microenvironment chemokine gradients within the unique spatial topography and temporal influences within heterogenous tumors receptor activation influence the signaling machinery that drive cellular movement into and out of the tumor Brian T Craig, Michael B Dwinell Tags Chemokine receptor; cell migration; immuno-oncology; metastasis; tumorigenesis

< GPCR News < GPCRs in Oncology and Immunology Noval insights and therapeutic strategies for tumor-induced antidiuretic hormones in Drosophila models has provided valuable insights into the mechanisms underlying tumor-induced insights could contribute to the advancement of diagnostic and therapeutic strategies for treating tumor-related

approach to treating patients suffering from lung cancer is to target surface receptors overexpressed on tumor cells, such as GPCR-family kinin receptors, and proteases that control tumor progression, such as kallikrein-related cancers, such as prostate and ovarian cancer, facilitating the invasive and metastatic capacity of tumor of KLKs in this neoplasm are modulated by the secretome of the different cell types present in the tumor microenvironment, the cancer subtype and the tumor stage, among others.

News < GPCRs in Oncology and Immunology GPR4 in the pH-dependent migration of melanoma cells in the tumor In melanoma as well as in other cancers, acidification of the tumor microenvironment (= TME, inverse pH-gradient) is a well-known driver of tumor progression and metastasis. Results indicate that GPR4 is involved in the migration of melanoma cells, especially in the tumor periphery

As a member of the GPCR family, G protein-coupled receptor 37 (GPR37) exhibits unknown functions in tumors The study explored the influence of GPR37 on tumor cell proliferation. Furthermore, we examined the effects of GPR37 on tumor cell apoptosis and invasion. migration, and proliferation, suppresses cell apoptosis, heightens resistance to cisplatin, and promotes tumor migration, and proliferation, promotes cell apoptosis, increases sensitivity to cisplatin, and affects tumor

SCD1 axis Published date September 21, 2024 Abstract "Colorectal cancer (CRC) is a prevalent malignant tumor Depletion of GPR37 significantly reduced CRC tumor cell growth both in vitro and in vivo. Mechanistic studies have shown that GPR37 modulates lipid metabolism in tumor cells by promoting SCD1

Consistent with GAL2 receptor-mediated tumor inhibition, for PDAC, survival is much higher for patients AT2R is interacting with four tumor suppressor proteins, Src homology phosphatase 1, Src homology phosphatase Pathways linked to these tumor suppressor proteins may enhance immune surveillance, prevent carcinogenesis

and clinical characterization of GH-producing pituitary adenomas/somatotroph pituitary neuroendocrine tumors characteristics of growth hormone (GH)-producing pituitary adenomas/somatotroph pituitary neuroendocrine tumors the GH change rate in the octreotide loading test, and WWC3, SERINC1, and ZFAND3 correlated with the tumor

Increased VIPR2 also exacerbated intraperitoneal proliferation of breast cancer MDA-MB-231 cells in a tumor Moreover, an inhibitor of mitogen-activated protein kinase kinase, U0126, attenuated tumor proliferation Together, these findings suggest that VIPR2 controls breast tumor growth by regulating the cAMP/PKA/ERK

Despite their crucial role in regulating antitumor immunity and tumorigenesis, therapeutic applications Specifically, the review highlights five GPCRs able to orchestrate tumor immunobiology at three main levels: tumor immunity, cancer cell expansion, and blood vessel development.

A defining hallmark of GBM is a highly acidic tumor microenvironment, which is thought to activate pro-tumorigenic This acidification is the result of altered tumor metabolism favoring aerobic glycolysis, a phenomenon Low extracellular pH confers radioresistant tumors to glial cells. However, the role of tumor microenvironment acidification in GPR68 activation has not been assessed in Conclusion: These results indicate GPR68 emerges as a critical sensor for an autocrine pro-tumorigenic

Trabecular Identity Abhishek Kumar Singh Investigating The Role of ADGRB3 Loss of Expression in Brain Tumor Glioblastoma (GBM) is the most prevalent central nervous system tumor in LFS, with TP53 mutations detected member of the BAI1-3 subfamily of adhesion GPCRS, has been observed to have low expression in brain tumors These observations lead me to hypothesize that ADGRB3 functions as a tumor suppressor in the brain, and Standard of care for MB includes tumor resection, chemotherapy, and cranio-spinal radiation.

Background: About one-third of patients with estrogen receptor alpha (ERα)-positive breast cancer have tumors Patients with ERα-positive/PR-negative tumors have shorter disease-free and overall survival than patients with ERα-positive/PR-positive tumors. Many of the genes affected by PR are part of central biological processes of tumorigenesis."

date October 13, 2023 Abstract "Background: Gliomas are the most frequently diagnosed primary brain tumors relationship between GPR37 gene expression and the clinicopathological factors, patient prognosis, tumor-infiltrating value, clinical relevance, and molecular function of GPR37 in glioma using TCGA, STRING, cBioPortal, Tumor

with the IFNγ stimulated/unstimulated HeLa S3 cells Since both TGFβ and IFNγ play an essential role in tumorigenesis both as a tumor promoter and tumor suppressor and known to antagonize each other's signalling, it would

demonstrated that the AT 2 R expression is reduced in human colorectal cancer and in stroma when compared to tumor Namsolleck , L de Vries , G N Moll Tags AT(2)R , Agonist , Angiotensin , Cancer , GPCR , Lanthionine , Tumor

of survival and immunotherapy response by the combined classifier of G protein-coupled receptors and tumor Jianying Gu Tags G protein-coupled receptors , Immunotherapy , Melanoma , Multi-omics , Pan-cancer , Tumor

GPR81 KD increased spheroid necrosis, reduced invasion and in vivo tumor growth, and altered expression F Pedersen Tags EPHA7 , Extracellular matrix , HCAR1 , Metabolite GPCR , Notch , PCDH7 , Spheroid , Tumor

Invasive procedures alone are not effective at completely removing such tumors. Within this dataset, we observed the association in the tumor microenvironment between the gene expression