2022
DOI: 10.1186/s13046-022-02457-4
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Revealing the crosstalk between nasopharyngeal carcinoma and immune cells in the tumor microenvironment

Abstract: Nasopharyngeal carcinoma (NPC) arises from the epithelial cells located in the nasopharynx and has a distinct geographic distribution. Chronic Epstein-Barr virus (EBV) infection, as its most common causative agents, can be detected in 100% of NPC types. In-depth studies of the cellular and molecular events leading to immunosuppression in NPC have revealed new therapeutic targets and diverse combinations that promise to benefit patients with highly refractory, advanced and metastatic NPC. This paper reviews the… Show more

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Cited by 19 publications
(12 citation statements)
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“…It should be noted that either the differentiated or undifferentiated subtype generally has a certain number of spindle cells (sarcoma-like) (8,13), which tend to cause erosion of surrounding tissue (9) and predominantly present in the invasive front or infiltrating the stroma (14,15). On the other side, the NPC microenvironment is highly heterogeneous with tumor stroma reaction (9), biotic components comprise of cancer-associated fibroblasts (CAFs), immune cells and endothelial cells, and abiotic components include extracellular matrix (ECM), cytokines, nutrients (8,12,16). Together, we can postulate that this variety of cancer cell subtypes, cooperating and competing with each other and interacting within their habitats spatiotemporally in the whole ecosystem of a high degree of genetic and phenotypic diversity, that jointly contribute to both malignant progression and clinical practise in NPC patients.…”
Section: Npc As Pathological Ecosystem Of "Unity Of Ecology and Evolu...mentioning
confidence: 99%
See 2 more Smart Citations
“…It should be noted that either the differentiated or undifferentiated subtype generally has a certain number of spindle cells (sarcoma-like) (8,13), which tend to cause erosion of surrounding tissue (9) and predominantly present in the invasive front or infiltrating the stroma (14,15). On the other side, the NPC microenvironment is highly heterogeneous with tumor stroma reaction (9), biotic components comprise of cancer-associated fibroblasts (CAFs), immune cells and endothelial cells, and abiotic components include extracellular matrix (ECM), cytokines, nutrients (8,12,16). Together, we can postulate that this variety of cancer cell subtypes, cooperating and competing with each other and interacting within their habitats spatiotemporally in the whole ecosystem of a high degree of genetic and phenotypic diversity, that jointly contribute to both malignant progression and clinical practise in NPC patients.…”
Section: Npc As Pathological Ecosystem Of "Unity Of Ecology and Evolu...mentioning
confidence: 99%
“…So the point I'm emphasizing here is that the great majority of these hallmarks ultimately affect cancer cell fitness through the ability of survival and/or reproduction (Figure 1). Most of hallmark phenotypic features governed by the crosstalk between cancer cells and tumor microenvironment in NPC have also been explored in more recent years (8,16,(32)(33)(34)(35)(36)43,44). Here I'd like to emphasize that, "nothing in evolution makes sense except in the light of tumor microenvironment".…”
Section: Npc As Pathological Ecosystem Of "Unity Of Ecology and Evolu...mentioning
confidence: 99%
See 1 more Smart Citation
“…22 Moreover, tumor immune microenvironment changes are closely associated with inflammatory and immune cell distribution in the peripheral blood. 23,24 Some studies have suggested that abnormal changes in systemic inflammatory cells, such as neutrophils, monocytes, and lymphocytes, are linked to the prognosis of many malignancies. Neutrophils could influence tumor development and progression via promoting tumor angiogenesis, aiding tumor cells to evade immune surveillance, and secreting large amounts of reactive oxygen species and nitric oxide.…”
Section: Discussionmentioning
confidence: 99%
“…Recruitment of immune cells, both immunostimulating and immunosuppressive, is mediated in part by increased expression of chemokines by tumour cells, macrophages, and dendritic cells ( Chen et al, 2020 ). Immune escape can be mediated by direct communication between the tumour and immune cells, for instance via inhibitory ligands/receptors and/or mutations of antigen presentation machinery, and/or indirect communication through chemokines/cytokines ( Jiang and Ying, 2022 ).
Fig.
…”
Section: Features Of the Time In Npcmentioning
confidence: 99%