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Tumor Microenvironment Characterization in Gastric Cancer Identifies Prognostic and Immunotherapeutically Relevant Gene Signatures
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Abstract
Tumor microenvironment (TME) cells constitute a vital element of tumor tissue. Increasing evidence has elucidated their clinicopathologic significance in predicting outcomes and therapeutic efficacy. Nonetheless, no studies have reported a systematic analysis of cellular interactions in the TME. In this study, we comprehensively estimated the TME infiltration patterns of 1,524 gastric cancer patients and systematically correlated the TME phenotypes with genomic characteristics and clinicopathologic features of gastric cancer using two proposed computational algorithms. Three TME phenotypes were defined, and the TMEscore was constructed using principal component analysis algorithms. The high TMEscore subtype was characterized by immune activation and response to virus and IFNγ. Activation of transforming growth factor β, epithelial–mesenchymal transition, and angiogenesis pathways were observed in the low TMEscore subtype, which are considered T-cell suppressive and may be responsible for significantly worse prognosis in gastric cancer [hazard ratio (HR), 0.42; 95% confidence interval (CI), 0.33–0.54; P < 0.001]. Multivariate analysis revealed that the TMEscore was an independent prognostic biomarker, and its value in predicting immunotherapeutic outcomes was also confirmed (IMvigor210 cohort: HR, 0.63; 95% CI, 0.46–0.89; P = 0.008; GSE78220 cohort: HR, 0.25; 95% CI, 0.07–0.89; P = 0.021). Depicting a comprehensive landscape of the TME characteristics of gastric cancer may, therefore, help to interpret the responses of gastric tumors to immunotherapies and provide new strategies for the treatment of cancers.
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“Recent studies reported that alteration of tumour immune microenvironment in gastric cancer is a pivotal strategy for predicting the immunotherapeutic responses and prognosis, which might provide new treatment strategies for patients [26, 27].”
From Phosphoserine phosphatase as a prognostic biomarker in patients with gastric cancer and its potential association with immune cells (2022) · cites this paper as [27]
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“The TME plays an important role in tumor progression and has an impact on the prediction of tumor prognosis.(30,31) Illustrating the fraction of stromal/immune cells could demonstrate the role of the TME in cancer and prognostic prediction.”
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“These signature not only affect the prognosis of gastric cancer patients, but also affect the efficacy of chemotherapy, immunotherapy and other treatments for patients with gastric cancer 36–38 .”
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“Last, we applied an equation similar to the previous study (Sotiriou et al., 2006; Zeng et al., 2019) to define the metabolic score:”
MethodA systematic pan-cancer analysis of PXDN as a potential target for clinical diagnosis and treatment
Zhou, X., Sun, Q., Xu, C., Zhou, Z., Chen, X., Zhu, X., Huang, Z., Wang, W., & Shi, Y. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.952849 · Cited by 18
“Zeng and his colleagues (including those related to immune-related pathways, epithelialmesenchymal transformation, and DNA loss and repair pathways) (14), and obtained a correlation between PXDN gene expression and the score of different gene sets in turn; these results were then visualized using the R package “ggplot…”
MethodLi, H., Lin, D., Yu, Z., Li, H., Zhao, S., Hainisayimu, T., Liu, L., & Wang, K. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.947802 · Cited by 18
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“Based on gene expression profiles, a recent study employed computational algorithms to predict immune-checkpoint blockade responses by estimating TME infiltration patterns of 1,524 tumors among gastric cancer patients (14).”
MethodSelf-citationZeng, W., Wang, J., Yang, J., Chen, Z., Cui, Y., Li, Q., Luo, G., Ding, H., Ju, S., Li, B., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1217590 · Cited by 18
Immune Cells in the Tumor Microenvironment of Soft Tissue Sarcomas
Jumaniyazova, E. D., Lokhonina, А. V., Dzhalilova, D. S., Kosyreva, A. M., & Fatkhudinov, T. (2023) · Cancers · doi:10.3390/cancers15245760 · Cited by 20
A signature of 17 immune-related gene pairs predicts prognosis and immune status in HNSCC patients
Jiang, P., Li, Y., Xu, Z., & He, S. (2020) · Translational Oncology · doi:10.1016/j.tranon.2020.100924 · Cited by 18
Yu, W., Chen, G., Yan, J., Wang, X., Zhu, Y., & Zhu, L. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03411-w · Cited by 19
“comprehensively described all the characteristics of the gastric cancer microenvironment and made a detailed analysis of immune infiltration [20].”
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“Patients with different immune infiltration conditions show differing clinical and immunotherapeutic benefits (Zeng et al., 2019; Lebid et al., 2020).”
BackgroundA large histological images dataset of gastric cancer with tumour microenvironment annotation for AI
Lou, S., Ji, J., Li, H., Zhang, X., Jiang, Y., Hua, M., Chen, K., Ge, K., Zhang, Q., Wang, L., et al. (2025) · Scientific Data · doi:10.1038/s41597-025-04489-9 · Cited by 18
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“…of gene sets that deposited genes associated with some biological processes were extracted from Mariathasan ’ s literature [25] and Zeng ’ s literature [26] , including epithelial-mesenchymal transition (EMT) markers, angiogenesis signature, TGF β /EMT markers, and immune activation signature.”
MethodXie, Y., Chen, H., Tian, M., Wang, Z., Wang, L., Zhang, J., Wang, X., & Lian, C. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1460547 · Cited by 17
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PCMT1 Is a Potential Prognostic Biomarker and Is Correlated with Immune Infiltrates in Breast Cancer
Guo, J., Du, X., & Li, C. (2022) · BioMed Research International · doi:10.1155/2022/4434887 · Cited by 17
“SIGLEC15, IDO1, CD274, HAVCR2, PDCD1, CTLA4, LAG3, and PDCD1LG2 are transcripts related to immune checkpoints [21].”
BackgroundNeurexophilin 4 is a prognostic biomarker correlated with immune infiltration in bladder cancer
Sun, X., Xin, S., Jin, L., Zhang, Y., & Ye, L. (2022) · Bioengineered · doi:10.1080/21655979.2022.2085284 · Cited by 17
“Computer algorithms for transcriptomic data are now being widely used to determine dynamic immune components in TME of tumor patients [20,34].”
MethodShen, Y., Li, X., Wang, D., Zhang, L., Li, X., Su, L., Fan, X., & Yang, X. (2022) · Cancer Medicine · doi:10.1002/cam4.5170 · Cited by 17
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“Three TME phenotypes were defined, and the TME score was constructed using principal component analysis algorithms according to previous work (25).”
MethodMo, S., Jin, B., Tseng, Y., Lin, L., Lin, L., Shen, X., Song, H., Kong, M., Luo, Z., Chu, Y., et al. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04326-w · Cited by 17
“biomarkers Boruta package was employed for the dimension reduction which applied the random forest algorithm to extract features and the order of them was scrambled to calculate the importance of features [26].”
MethodYu, P., Ding, G., Huang, X., Wang, C., Fang, J., Huang, L., Ye, Z., Xu, Q., Wu, X., Yan, J., et al. (2024) · International Journal of Surgery · doi:10.1097/js9.0000000000001281 · Cited by 17
“TMEscore A was associated with immune-related signatures, while TMEscore B was associated with stromal-relevant signatures [25] .”
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ARHGAP11A Is a Prognostic Biomarker and Correlated With Immune Infiltrates in Gastric Cancer
Fan, B., Ji, K., Bu, Z., Zhang, J., Yang, H., Li, J., & Wu, X. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.720645 · Cited by 17
“Studies have shown that the tumor immune infiltrates correlated with prognosis and response to therapy (Zeng et al., 2019; Refolo et al., 2020).”
BackgroundSelf-citationWang, W., Ye, Y., Zhang, X., Sun, W., & Bao, L. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e13989 · Cited by 17
“Molecular subtypes of tumours are associated with patient clinical outcomes and the TIME [63].”
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“In line with prior researches, our findings confirm the existence of histology-specific immunoregulatory mechanisms in GC [32, 33].”
Zhang, L., Li, L., Zhan, Y., Zhu, Z., & Zhang, X. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.607090 · Cited by 15
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“We then curated the final genes determined to conduct principal component analysis (PCA), and principal component 1 and 2 were extracted to construct the m(6)A score (44, 45).”
MethodYang, Y., Liang, J., Zhao, J., Wang, X., Feng, D., Xu, H., Shen, Y., Zhang, Y., Dai, J., Wang, Z., et al. (2023) · Diagnostic Pathology · doi:10.1186/s13000-023-01384-y · Cited by 16
“Meanwhile, we picked SIGLEC15, TIGIT, CD274, HAVCR2, PDCD1, CTLA4, LAG3 and PDCD1LG2 as immune checkpoint-associated transcripts [47–49].”
Sha, R., Dong, X., Yan, S., Dai, H., Sun, A., You, L., & Guo, Z. (2024) · Scientific Reports · doi:10.1038/s41598-024-52638-8 · Cited by 16
Identification of New Therapeutic Targets for Gastric Cancer With Bioinformatics
Yang, L., Wang, J., Zhang, T., Wang, H., & Li, L. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00865 · Cited by 16
“Studies have found that higher TME scores show improved immune treatment and prognosis (Junttila and de Sauvage, 2013; Lazar et al., 2018; Zeng et al., 2019).”
Association of the Psoriatic Microenvironment With Treatment Response
Wang, G., Miao, Y., Kim, N., Sweren, E., Kang, S., Hu, Z., & Garza, L. A. (2020) · JAMA Dermatology · doi:10.1001/jamadermatol.2020.2118 · Cited by 16
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Pan-Cancer Analysis Predicts FOXS1 as a Key Target in Prognosis and Tumor Immunotherapy
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“method, a previous study was employed as a reference to investigate TME-related biological processes.(13) Next, based on the TCGA database, we exploited the “Immune Gene” module of the TIMER2, ImmuCellAI platform, and referred to a previous study to estimate the relationship between FOXS1 expression and immune cell in…”
BackgroundMethodShen, X. P., Zhong, J., He, J., Han, J., & Chen, N. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.978092 · Cited by 16
Wang, K.-W., Wang, M.-D., Li, Z.-X., Hu, B.-S., Wu, J.-J., Yuan, Z.-D., Wu, X., Yuan, Q.-F., & Yuan, F.-L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.992060 · Cited by 16
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“included several genomic and transcriptomic datasets from patients with different cancer types treated with immunotherapy in their study to evaluate the efficiency of the tumor microenvironment score they developed in predicting the immunotherapeutic benefits (71).”
Self-citationHuang, M.-Y., Liu, X.-Y., Shao, Q., Zhang, X., Miao, L., Wu, X.-Y., Xu, Y.-X., Wang, F., Wang, H.-Y., Zeng, L., et al. (2022) · BMC Gastroenterology · doi:10.1186/s12876-021-02073-0 · Cited by 15
“Recent studies reported that alteration of tumour immune microenvironment in gastric cancer is a pivotal strategy for predicting the immunotherapeutic responses and prognosis, which might provide new treatment strategies for patients [26, 27].”
BackgroundSang, S., Sun, Z., Zheng, W., Wang, W., Islam, M. T., Chen, Y., Yuan, Q., Cheng, C., Xi, S., Han, Z., et al. (2025) · Cell Reports Medicine · doi:10.1016/j.xcrm.2025.102242 · Cited by 15
“21,24 27 Therefore, developing a non-invasive and cost-effective model to assess chemotherapy response while integrating TME status to enhance model performance is imperative.”
Gou, Q., Liu, Z., Xie, Y., Deng, Y., Ma, J., Li, J., & Zheng, H. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.995555 · Cited by 15
“A previous study depicted a vast TME landscape of gastric cancer and helped to provide new strategies for interpreting responses to immunotherapies (Zeng et al., 2019).”
BackgroundZeng, J., Tan, H., Huang, B., Zhou, Q., Ke, Q., Dai, Y., Tang, J., Xu, B., Feng, J., & Yu, L. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.959170 · Cited by 15
“gz) were processed according to previous studies (Zeng et al., 2019; Chen et al., 2021).”
MethodGene signature developed for predicting early relapse and survival in early-stage pancreatic cancer
Huang, L., Yuan, X., Zhao, L., Han, Q., Yan, H., Yuan, J., Guan, S., Xu, X., Dai, G., Wang, J., et al. (2023) · BJS Open · doi:10.1093/bjsopen/zrad031 · Cited by 15
Chen, Z., Li, Q., Lin, Y., Lin, S., Gao, J., & Chen, S. (2023) · Scientific Reports · doi:10.1038/s41598-023-37300-z · Cited by 16
Nie, K., Zheng, Z., Li, J., Chang, Y., Deng, Z., Huang, W. J., & Li, X. (2023) · The FASEB Journal · doi:10.1096/fj.202301249r · Cited by 15
Qian, C., Jiang, H., Peng, Z., Sun, X., & Zhang, J. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1435334 · Cited by 15
Self-citationMa, J., Hu, X., Yao, Y., Wu, L., Sheng, C., Chen, K., & Liu, B. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.756193 · Cited by 15
“The advantage of this method is that the score is concentrated on the set with the largest block of well-correlated (or anticorrelated) genes in the set, while down-weighting contributions from genes that do not track with other set members (28, 29): ferroptosis score= ∑ (PC1i + PC2i) where i is the expression of subt…”
MethodHan, S., Qi, J., Fang, K., Wang, H., Tang, Y., Wu, D., & Han, Y. (2022) · Cancer Medicine · doi:10.1002/cam4.4531 · Cited by 14
Xu, L., Hu, Y., & Liu, W. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s349186 · Cited by 15
Liu, J., Zhang, Z., Zhang, W., Meng, L., Wang, J., Lv, Z., Xia, H., Wu, M. Y., Zhang, Y., & Wang, J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.791630 · Cited by 16
Wang, L., Liu, Z., Zhu, R., Liang, R., Wang, W., Li, J., Zhang, Y., Guo, C., Han, X., & Sun, Y. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.02.031 · Cited by 15
“The similar methods have also been implemented and validated in gastric and colorectal cancer [28,29].”
MethodXie, Y., Xiao, L., Chen, L., Zheng, Y., Zhang, C., & Wang, G. (2021) · Genes · doi:10.3390/genes12020178 · Cited by 17
“Integrated analyses of other omics are also common in medical research, namely, multi-genome [51], and multi-transcriptome [52] analyses.”
BackgroundGong, S., Wu, C., Köhler, F., Meixensberger, J., Schopow, N., & Kallendrusch, S. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.838548 · Cited by 16
“We considered CXCL10, CXCL9, GZMA, GZMB, PRF1, CD8A, TBX2, and TNF as immune-activating transcripts; IDO1, CD274, HAVCR2, PDCD1, CTLA4, LAG3, and PDCD1LG2 as immune checkpoint transcripts; and VIM, ACTA2, COL4A1, TGFBR2, ZEB1, CLDN3, SMAD9, TWIST1, and TGRB1 as transforming growth factor (TGF)β/epithelial-mesenchymal…”
Jiang, Y., Mai, G., Zhao, X., Tang, M. X., Yang, P., Cheng, Q., Tian, H., Niu, Z., Wang, X., Wang, J., et al. (2025) · npj Precision Oncology · doi:10.1038/s41698-025-01087-1 · Cited by 15
“In immune in fi ltration analysis, low-risk patients show higher levels of CD4/CD8 T cells and Treg cells, which correlate with better prognosis across various cancers 31,32 .”
G Protein‐Coupled Receptor Signaling: Implications and Therapeutic Development Advances in Cancers
Khan, I. R., Khurshid, S., Almawash, S., Kumar, R., Akil, A. A., Bhat, A. A., & Macha, M. A. (2025) · MedComm · doi:10.1002/mco2.70375 · Cited by 15
Precision oncology in gastric cancer: Shaping the future of personalized treatment
Migliore, C., Fenocchio, E., Giordano, S., & Corso, S. (2025) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2025.103038 · Cited by 14
“Zeng and colleagues, using computational algorithms, analyzed the expression profile of more than 1500 gastric tumors and identified three distinct patterns of tumor TME infiltration, each characterized by a peculiar proportion of cancer-associated fibroblasts (CAF) and leukocytes [43].”
Dong, M., Cui, X., Wang, G., Zhang, Q., & Li, X. (2022) · Aging · doi:10.18632/aging.204158 · Cited by 14
“Finally, the m6Ascore was determined in a manner similar to the Genomic Grade Index (GGI) [21]: riskScore = ∑ (PC1i + PC2i), where i was the expression of overlapping IRGs with a significant difference in prognosis of BC patients.”
MethodXiao, Y., Jiang, J., Chen, Y., Huang, Y., & Wei, C. (2022) · ONCOLOGIE · doi:10.32604/oncologie.2022.026118 · Cited by 14
Gao, L., Ying, F., Cai, J., Peng, M., Xiao, M., Sun, S., Zeng, Y., Xiong, Z., Cai, L., Gao, R., et al. (2023) · Journal of Ovarian Research · doi:10.1186/s13048-022-01065-2 · Cited by 15
“We performed a systematical search for immune checkpoint genes, immune chemokines, interleukin, interferon as well as epithelial-mesenchymal transition (EMT) -related genes, which were extracted to explore their relationship with Pyrsig score [35].”
MethodBai, M., & Liu, X. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1191009 · Cited by 14
Tang, L., Zhang, W., Qi, T., Jiang, Z., & Tang, D. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-024-02009-7 · Cited by 14
Liu, X., Cao, Y., Lv, K., Gu, Y., Jin, K., He, X., Fang, H., Fei, Y., Shi, M., Lin, C., et al. (2020) · OncoImmunology · doi:10.1080/2162402x.2020.1845038 · Cited by 14
“This may, partly, be attributed to the heterogeneous TME, T-cellinflamed gene-expression profile and different molecular subtypes.(15,16) Consequently, in order to further improve response rates and expand therapeutic effects, novel predictive biomarkers and potential immunoevasive mechanisms should be identified in g…”
BackgroundSelf-citationYang, M., Chen, G., Gao, K., & Wang, Y. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.622752 · Cited by 14
“2e-16; Figure 2C), suggesting T cell activation and effective immune response in C2 (39, 40).”
BackgroundZhu, M., Cui, Y., Mo, Q., Zhang, J., Zhao, T., Xu, Y.-J., Wu, Z., Sun, D., Zhang, X., Li, Y., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.782551 · Cited by 14
“This method minimized the deprivation of information contained in the original index and reduced the indicators to be analyzed, thereby allowing a comprehensive analysis of the collected data; lastly, the m(6)A score was defined by performing a formula similar to that used in previous studies (48, 49).”
MethodSelf-citationWang, H., Wu, J., Ling, R., Li, F., Yang, Q., He, J., Lei, X., Wu, C., Zhang, G., Zheng, B., et al. (2022) · Molecular Therapy — Oncolytics · doi:10.1016/j.omto.2022.01.008 · Cited by 14
“Several studies have reported that the heterogeneity of the immune microenvironment within and among individual tumors is greatly responsible for such variations of treatment responses and patient outcomes.(7,8) For example, the tumor environment context observed at initially diagnosis could reflect the immune respons…”
BackgroundLiu, Y., Zheng, S., Wang, T., Fang, Z., Kong, J., & Liu, J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.842220 · Cited by 14
“The m5Cscore was defined using a method similar to the Genomic Grade Index (GGI) (Sotiriou et al., 2006; Zeng et al., 2019):”
MethodLuo, Y., Zong, Y., Hua, H., Gong, M., Peng, Q., Li, C., Neculai, D., & Zeng, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1011590 · Cited by 15
Yao, Y., Chen, H., Lou, M., & Chen, T. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1071694 · Cited by 14
“Referring to some high-quality literatures, the expression differences of immune checkpoint related genes (SIGLEC15, TIGIT, CD274, HAVCR2, PDCD1, CTLA4, LAG3 and PDCD1LG2) were compared between these two groups by “ggplots2” and “pheatmap” R packages (Ravi et al., 2018; Wang et al., 2019; Zeng et al., 2019; Yi et al.,…”
ResultSkubleny, D., Lin, A., Garg, S., McLean, R., McCall, M., Ghosh, S., Spratlin, J. L., Schiller, D., & Rayat, G. R. (2023) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v15.i2.303 · Cited by 14
Song, Y., Sun, Y., Sun, T., & Tang, R. (2020) · Combinatorial Chemistry & High Throughput Screening · doi:10.2174/1386207323666200407075004 · Cited by 14
Luo, T., Du, Y., Duan, J., Liang, C., Chen, G., Jiang, K., Chen, Y., & Chen, Y. (2020) · Technology in Cancer Research & Treatment · doi:10.1177/1533033820971670 · Cited by 14
“In GC, the crosstalk between immune cells and tumor cells plays a vital role in predicting prognosis and immunotherapeutic outcomes.(29) After comparing the difference of tumorinfiltrating immune cells between high- and low-risk groups, we observed a high level of T cells gamma delta, monocytes, macrophages M2, and ma…”
BackgroundA signature of 24 aging‑related gene pairs predict overall survival in gastric cancer
Zhang, Y., Yan, Y., Ning, N., Shen, Z., & Ye, Y. (2021) · BioMedical Engineering OnLine · doi:10.1186/s12938-021-00871-x · Cited by 14
“on the role of tumor immune infiltrating cells in GC suggest that it can be used as independent prognostic markers [37, 38].”
Background
Metadata
- Authors
- Zeng, D., Li, M., Zhou, R., Zhang, J., Sun, H., Shi, M., Bin, J., Liao, Y., Rao, J., & Liao, W.
- Affiliations
- Nanfang Hospital (CN)
- Southern Medical University (CN)
- ORCID
- Venue
- Cancer Immunology Research
- Published
- 2019-05-01
- Volume
- 7
- Issue
- 5
- Pages
- 737-750
- ISSN
- 2326-6066 (ISSN-L)
- 2326-6074
- OpenAlex
- W2920600229
- Semantic Scholar
- 180648d1827a7e8c086f03b00ca69831a1ca538e
- Cited by
- 986
- References
- 76
- Citations by year
- 2026: 38 · 2025: 87 · 2024: 164 · 2023: 211 · 2022: 251 · 2021: 162 · 2020: 64 · 2019: 9
- FWCI
- 53.10
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cancer Immunology Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Natural Science Foundation of China (81772580)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Health Sciences › Medicine › Oncology › Gastric Cancer Management and Outcomes
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Keywords
- gastric cancer, tumor microenvironment, prognostic factors, immunotherapy response, immune cell infiltration, T cell suppression, epithelial-mesenchymal transition, angiogenesis, TGF-beta signaling, IFN-gamma response, gene expression signatures, IMvigor210
- MeSH terms
- Antineoplastic Agents, Immunological, Algorithms, Humans, Immunotherapy, Phenotype, Prognosis, Stomach Neoplasms, Gene Expression Regulation, Neoplastic, Tumor Microenvironment
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