# The Bioinformatics and Experimental Analysis of CD276 for Prognosis and Immune Infiltrates in Colon Adenocarcinoma

**Authors:** Rui Chen, Tao Zhang, Jingru Yang, Longxia Zhang, Fei Su

PMC · DOI: 10.1002/cnr2.70503 · Cancer Reports · 2026-02-22

## TL;DR

This study explores the role of CD276 in colon adenocarcinoma, linking its high expression to poor prognosis and immune infiltration.

## Contribution

The study identifies CD276 as a novel prognostic biomarker and immune-related factor in colon adenocarcinoma.

## Key findings

- CD276 expression is significantly elevated in colon adenocarcinoma (p < 0.0001).
- High CD276 levels correlate with microsatellite instability, survival, and disease progression.
- CD276 is associated with immune cell infiltration and immune checkpoint expression.

## Abstract

Colon adenocarcinoma (COAD), although the third‐most common type of gastrointestinal tumors, still lacks specific biomarkers for early diagnosis, treatment, and prognosis.

This study aimed to evaluate the CD276 in tumorigenesis, prognosis and immunity for colon adenocarcinoma.

The CD276 expression in colon adenocarcinoma was established by using RNA‐sequencing transcriptomic data of The Cancer Genome Atlas (TCGA) databases. The biological functions of CD276 were evaluated using the Metascape database and Gene Set Enrichment Analysis (GSEA). The association between CD276 and immune cell infiltration was investigated by TIMER website. Correlation analysis was performed between CD276 expression and clinicopathological characteristics. CD276 expression was significantly elevated in colon adenocarcinoma tumor (p < 0.0001). High CD276 was associated with microsatellite instability (MSI) status, patients' survival, and disease progression. Cox regression analysis revealed that CD276 was a risk factor for overall survival [hazard ratio (HR): 1.848, p = 2.64E−03], disease‐specific survival (HR: 2.406, p = 5.35E−04), and progression‐free interval (HR: 1.772, p = 2.04E−03). Moreover, CD276 level was significantly associated with tumor immune cell infiltration, biomarkers of immune cells, and immune checkpoint expression.

Our analyses indicated that increased CD276 may contribute to colon adenocarcinoma development by activating tumor‐promoting signal pathways and altering the immune microenvironment.

## Linked entities

- **Genes:** CD276 (CD276 molecule) [NCBI Gene 80381]
- **Diseases:** colon adenocarcinoma (MONDO:0002271)

## Full-text entities

- **Genes:** CBL (Cbl proto-oncogene) [NCBI Gene 867] {aka C-CBL, CBL2, FRA11B, NSLL, RNF55}, KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, MS4A4A (membrane spanning 4-domains A4A) [NCBI Gene 51338] {aka 4SPAN1, CD20-L1, CD20L1, HDCME31P, MS4A4, MS4A7}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, CD28 (CD28 molecule) [NCBI Gene 940] {aka IMD123, Tp44}, CD163 (CD163 molecule) [NCBI Gene 9332] {aka M130, MM130, SCARI1}, RBBP4 (RB binding protein 4, chromatin remodeling factor) [NCBI Gene 5928] {aka NURF55, RBAP48, lin-53}, NRP1 (neuropilin 1) [NCBI Gene 8829] {aka BDCA4, CD304, NP1, NRP, VEGF165R}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, LAG3 (lymphocyte activating 3) [NCBI Gene 3902] {aka CD223}, IRF5 (interferon regulatory factor 5) [NCBI Gene 3663] {aka SLEB10}, CD276 (CD276 molecule) [NCBI Gene 80381] {aka 4Ig-B7-H3, B7-H3, B7H3, B7RP-2}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, HLA-DPA1 (major histocompatibility complex, class II, DP alpha 1) [NCBI Gene 3113] {aka DP(W3), DP(W4), DPA1, HLA-DP1A, HLA-DPA, HLADP}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}, CCR7 (C-C motif chemokine receptor 7) [NCBI Gene 1236] {aka BLR2, CC-CKR-7, CCR-7, CD197, CDw197, CMKBR7}, PDCD1LG2 (programmed cell death 1 ligand 2) [NCBI Gene 80380] {aka B7DC, Btdc, CD273, PD-L2, PDCD1L2, PDL2}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, SRC (SRC proto-oncogene, non-receptor tyrosine kinase) [NCBI Gene 6714] {aka ASV, SRC1, THC6, c-SRC, p60-Src}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, HLA-DRA (major histocompatibility complex, class II, DR alpha) [NCBI Gene 3122] {aka HLA-DRA1}, PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743] {aka COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, HGF (hepatocyte growth factor) [NCBI Gene 3082] {aka DFNB39, F-TCF, HGFB, HPTA, SF}, TENM1 (teneurin transmembrane protein 1) [NCBI Gene 10178] {aka ODZ1, ODZ3, TEN-M1, TEN1, TNM, TNM1}, HLA-DQB1 (major histocompatibility complex, class II, DQ beta 1) [NCBI Gene 3119] {aka CELIAC1, HLA-DQB, IDDM1}, CD1C (CD1c molecule) [NCBI Gene 911] {aka BDCA1, CD1, R7}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, VSIG4 (V-set and immunoglobulin domain containing 4) [NCBI Gene 11326] {aka CRIg, Z39IG}, HLA-DPB1 (major histocompatibility complex, class II, DP beta 1) [NCBI Gene 3115] {aka DPB1, HLA-DP, HLA-DP1B, HLA-DPB}, IDO1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 3620] {aka IDO, IDO-1, INDO}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, ITGAM (integrin subunit alpha M) [NCBI Gene 3684] {aka CD11B, CR3A, HNA-4, MAC-1, MAC1A, MO1A}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, MAP2K7 (mitogen-activated protein kinase kinase 7) [NCBI Gene 5609] {aka JNKK2, MAPKK7, MEK, MEK 7, MKK7, PRKMK7}, ITGAX (integrin subunit alpha X) [NCBI Gene 3687] {aka CD11C, SLEB6}, CD8B (CD8 subunit beta) [NCBI Gene 926] {aka CD8B1, CD8beta, LEU2, LY3, LYT3, Ly-3}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, ZHX2 (zinc fingers and homeoboxes 2) [NCBI Gene 22882] {aka AFR1, RAF}
- **Diseases:** MSI-H (MESH:D053842), multiple myeloma (MESH:D009101), Cancer (MESH:D009369), death (MESH:D003643), CRC (MESH:D015179), metastasis (MESH:D009362), NSCLC (MESH:D002289), COAD (MESH:D003110), NES (MESH:C537354), instability (MESH:D043171), gastrointestinal tumors (MESH:D005770), carcinogenesis (MESH:D063646), breast cancer (MESH:D001943), GACs (MESH:D013274)
- **Chemicals:** pembrolizumab (MESH:C582435), puromycin (MESH:D011691), ROS (-), ipilimumab (MESH:D000074324), nivolumab (MESH:D000077594)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** 8A-C, AUC of 0, 2A-C
- **Cell lines:** SW620 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0547), SW480 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0546), HT-29 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0320), HCT116 — Homo sapiens (Human), Colon carcinoma, Cancer cell line (CVCL_0291), NCM-460 — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0460)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12928083/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12928083/full.md

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Source: https://tomesphere.com/paper/PMC12928083