# Colorectal cancer pathogenesis, oncogenic signaling networks and targeted therapeutic advances

**Authors:** Yue Chen, Jiaqi Zhang, Yi Ding, Fang Zhu, Yinnan Chen

PMC · DOI: 10.1186/s43556-026-00433-4 · Molecular Biomedicine · 2026-03-14

## TL;DR

This paper reviews colorectal cancer's development, key signaling pathways, and recent advances in targeted therapies to improve patient outcomes.

## Contribution

The paper provides a comprehensive overview of oncogenic signaling networks and evaluates current and emerging targeted therapies for colorectal cancer.

## Key findings

- Targeted therapies have improved CRC survival but are limited by complex molecular networks.
- Immune checkpoint inhibitors and tumor microenvironment insights are shaping new treatment strategies.
- Understanding signaling pathways enables the design of precise, personalized therapies.

## Abstract

Colorectal cancer (CRC) constitutes a prominent global health burden, being the third most frequently diagnosed malignancy in terms of incidence and the second leading cause of cancer-associated death across the globe. Malignant transformation of colonic epithelial cells stems from the intricate dysregulation of intracellular signal transduction networks. Although targeted therapies have substantially improved patient survival relative to traditional treatments, the complexity of the molecular networks driving carcinogenesis continues to limit the overall prognosis. This review delineates the core signaling cascades governing CRC initiation and progression, with emphasis on the molecular hallmarks of the disease. Drawing on a growing body of high-quality preclinical and clinical evidence, we summarize currently available targeted agents and critically evaluate their underlying mechanisms of action and clinical curative effects, and inherent limitations within the contemporary therapeutic landscape. In addition, we discuss how recent advances in immune checkpoint inhibitors (ICIs) along with a deeper understanding of the tumor microenvironment are shaping global clinical guidelines and revealing promising new targets and combinatorial strategies. In summary, expanding insights into oncogenic signaling pathways are guiding the development of novel treatments and enabling the identification of key elements amenable to pharmacological intervention. Ultimately, this review aims to support the rational design of precise and personalized therapeutic strategies to improve CRC prognosis.

## Linked entities

- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** Shc1 (src homology 2 domain-containing transforming protein C1) [NCBI Gene 20416] {aka Shc, ShcA, p66, p66shc}, STAT1 (signal transducer and activator of transcription 1) [NCBI Gene 6772] {aka CANDF7, IMD31A, IMD31B, IMD31C, ISGF-3, STAT91}, DPP7 (dipeptidyl peptidase 7) [NCBI Gene 29952] {aka DPP, DPP II, DPP2, DPPII, II, QPP}, EIF3H (eukaryotic translation initiation factor 3 subunit H) [NCBI Gene 8667] {aka EIF3S3, eIF3-gamma, eIF3-p40}, FASN (fatty acid synthase) [NCBI Gene 2194] {aka FAS, OA-519, SDR27X1}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, PRKAB1 (protein kinase AMP-activated non-catalytic subunit beta 1) [NCBI Gene 5564] {aka AMPK, HAMPKb}, USP19 (ubiquitin specific peptidase 19) [NCBI Gene 10869] {aka ZMYND9}, RASGRF1 (Ras protein specific guanine nucleotide releasing factor 1) [NCBI Gene 5923] {aka CDC25, CDC25L, GNRP, GRF1, GRF55, H-GRF55}, AZIN2 (antizyme inhibitor 2) [NCBI Gene 113451] {aka ADC, AZIB1, ODC-p, ODC1L, ODCp}, BTRC (beta-transducin repeat containing E3 ubiquitin protein ligase) [NCBI Gene 8945] {aka BETA-TRCP, FBW1A, FBXW1, FBXW1A, FWD1, bTrCP}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, GSDMC (gasdermin C) [NCBI Gene 56169] {aka MLZE}, MSH6 (mutS homolog 6) [NCBI Gene 2956] {aka GTBP, GTMBP, HNPCC5, HSAP, LYNCH5, MMRCS3}, CCND1 (cyclin D1) [NCBI Gene 595] {aka BCL1, D11S287E, PRAD1, U21B31}, Tfrc (transferrin receptor) [NCBI Gene 22042] {aka 2610028K12Rik, CD71, E430033M20Rik, Mtvr1, TFR, TFR1}, BCL9 (BCL9 transcription coactivator) [NCBI Gene 607] {aka LGS}, APC (APC regulator of Wnt signaling pathway) [NCBI Gene 324] {aka BTPS2, DESMD, DP2, DP2.5, DP3, GS}, ARRB1 (arrestin beta 1) [NCBI Gene 408] {aka ARB1, ARR1}, MET (MET proto-oncogene, receptor tyrosine kinase) [NCBI Gene 4233] {aka AUTS9, DA11, DFNB97, HGFR, RCCP2, c-Met}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, SREBF1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 6720] {aka HMD, IFAP2, SREBP1, bHLHd1}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, SLC2A3 (solute carrier family 2 member 3) [NCBI Gene 6515] {aka GLUT3}, NRP1 (neuropilin 1) [NCBI Gene 8829] {aka BDCA4, CD304, NP1, NRP, VEGF165R}, CHKA (choline kinase alpha) [NCBI Gene 1119] {aka CHK, CK, CKI, EK, NEDMIMS}, TBX21 (T-box transcription factor 21) [NCBI Gene 30009] {aka IMD88, T-PET, T-bet, TBET, TBLYM}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, PRRT2 (proline rich transmembrane protein 2) [NCBI Gene 112476] {aka BFIC2, BFIS2, DSPB3, DYT10, EKD1, FICCA}, ACOD1 (aconitate decarboxylase 1) [NCBI Gene 730249] {aka CAD, IRG1}, DLL1 (delta like canonical Notch ligand 1) [NCBI Gene 28514] {aka DELTA1, DL1, Delta, NEDBAS}, PTPN11 (protein tyrosine phosphatase non-receptor type 11) [NCBI Gene 5781] {aka BPTP3, CFC, JMML, METCDS, NS1, PTP-1D}, TNKS (tankyrase) [NCBI Gene 8658] {aka ARTD5, PARP-5a, PARP5A, PARPL, TIN1, TINF1}, NLRC4 (NLR family CARD domain containing 4) [NCBI Gene 58484] {aka AIFEC, CARD12, CLAN, CLAN1, CLANA, CLANB}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, RAF1 (Raf-1 proto-oncogene, serine/threonine kinase) [NCBI Gene 5894] {aka CMD1NN, CRAF, NS5, Raf-1, c-Raf}, CGAS (cyclic GMP-AMP synthase) [NCBI Gene 115004] {aka C6orf150, D4, MB21D1, h-cGAS}, GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], PTK2 (protein tyrosine kinase 2) [NCBI Gene 5747] {aka FADK, FADK 1, FAK, FAK1, FRNK, PPP1R71}, PECAM1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 5175] {aka CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM}, SOX2 (SRY-box transcription factor 2) [NCBI Gene 6657] {aka ANOP3, MCOPS3}, FGF1 (fibroblast growth factor 1) [NCBI Gene 2246] {aka AFGF, ECGF, ECGF-beta, ECGFA, ECGFB, FGF-1}, ERBB3 (erb-b2 receptor tyrosine kinase 3) [NCBI Gene 2065] {aka ErbB-3, FERLK, HER3, LCCS2, MDA-BF-1, VSCN1}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CCR5 (C-C motif chemokine receptor 5) [NCBI Gene 1234] {aka CC-CKR-5, CCCKR5, CCR-5, CD195, CKR-5, CKR5}, NOTCH4 (notch receptor 4) [NCBI Gene 4855] {aka INT3}, PIK3CD (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta) [NCBI Gene 5293] {aka APDS, IMD14, IMD14A, IMD14B, P110DELTA, PI3K}, SLITRK4 (SLIT and NTRK like family member 4) [NCBI Gene 139065], Kras (Kras proto-oncogene, GTPase) [NCBI Gene 16653] {aka K-Ras, K-Ras 2, K-ras, Ki-ras, Kras-2, Kras2}, VEGFD (vascular endothelial growth factor D) [NCBI Gene 2277] {aka FIGF, VEGF-D}, NRAS (NRAS proto-oncogene, GTPase) [NCBI Gene 4893] {aka ALPS4, CMNS, N-ras, NCMS, NRAS1, NS6}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, MEFV (MEFV innate immunity regulator, pyrin) [NCBI Gene 4210] {aka FMF, MEF, PAAND, TRIM20}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, TGM2 (transglutaminase 2) [NCBI Gene 7052] {aka G(h), TG(C), TGC, hTG2, tTG}, STK11 (serine/threonine kinase 11) [NCBI Gene 6794] {aka LKB1, PJS, hLKB1}, FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353] {aka AP-1, C-FOS, p55}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, FOSL1 (FOS like 1, AP-1 transcription factor subunit) [NCBI Gene 8061] {aka FRA, FRA1, fra-1}, BECN1 (beclin 1) [NCBI Gene 8678] {aka ATG6, VPS30, beclin1}
- **Diseases:** skin adverse (MESH:D012871), solid (MESH:D018250), Inflammation (MESH:D007249), CAC (MESH:D000083023), B-cell malignancies (MESH:D016393), vasomotor (MESH:D012223), colon (MESH:D003108), serous ovarian cancer (MESH:D010051), fatigue (MESH:D005221), ADCC (MESH:C565972), colitis (MESH:D003092), metastatic disease (MESH:D000092182), diarrhea (MESH:D003967), breast cancer (MESH:D001943), hyperglycemia (MESH:D006943), TI-HTN (MESH:D006973), NECD (MESH:C535509), MS (MESH:D009103), ulcerative colitis (MESH:D003093), MMR-deficient (MESH:C536928), Crohn's disease (MESH:D003424), Malignant (MESH:D009369), hand-foot reaction (MESH:D060831), melanoma (MESH:D008545), chromosomal abnormalities (MESH:D002869), proteinuria (MESH:D011507), CIMP (MESH:D007516), preeclampsia (MESH:D011225), NICD (MESH:D015270), invasive carcinoma (MESH:D009361), colon polyp (MESH:D003111), gastrointestinal toxicity (MESH:D005767), CRC (MESH:D015179), CMS (MESH:C535673), CIN (MESH:D043171), MDSCs (OMIM:601308), gastric cancer (MESH:D013274), dysplasia (MESH:D015792), WRN (MESH:D014898), HCC (MESH:D006528), Lynch syndrome (MESH:D003123), tumorigenic (MESH:D002471), Cytotoxicity (MESH:D064420), immune (MESH:D007154), NSCLC (MESH:D002289), carcinogenesis (MESH:D063646), bone disorders (MESH:D001847), death (MESH:D003643), hyperplastic polyp (MESH:D011127), liver metastasis (MESH:D009362), adenoma (MESH:D000236), MSI-H (MESH:D053842), infection (MESH:D007239), Adenoma-carcinoma (MESH:D000230), intestinal tumor (MESH:D007414), biliary tract cancer (MESH:D001661), IBD (MESH:D015212), serrated lesions (MESH:D009059)
- **Chemicals:** glucose (MESH:D005947), pembrolizumab (MESH:C582435), copanlisib (MESH:C000589253), nucleotide (MESH:D009711), BKM120 (MESH:C571178), everolimus (MESH:D000068338), rucaparib (MESH:C531549), faricimab (MESH:C000723200), XAV-939 (MESH:C544261), LGK974 (MESH:C586458), LY3214996 (MESH:C000719760), Trastuzumab deruxtecan (MESH:C000614160), Cobimetinib (MESH:C574276), Dabrafenib (MESH:C561627), ATP (MESH:D000255), panitumumab (MESH:D000077544), PX-866 (MESH:C496788), carbohydrate (MESH:D002241), 4-HPA (MESH:C008070), selumetinib (MESH:C517975), temozolomide (MESH:D000077204), GTP (MESH:D006160), SI (MESH:D012825), fiber (MESH:D004043), MK-8353 (MESH:C000632607), BMS-582664 (MESH:C509922), pertuzumab (MESH:C485206), atezolizumab (MESH:C000594389), bevacizumab (MESH:D000068258), avutometinib (MESH:C577924), reactive nitrogen species (MESH:D026361), ROS (MESH:D017382), vemurafenib (MESH:D000077484), phosphatidylinositol-3,4,5-trisphosphate (MESH:C060974), MEN1611 (MESH:C559137), Adagrasib (MESH:C000718190), fruquintinib (MESH:C000591844), HLX07 (MESH:C000722210), cetuximab (MESH:D000068818), duvelisib (MESH:C586691), 5-aminovaleric acid (MESH:C013809), anlotinib (MESH:C000625192), LGX818 (MESH:C000601108), ARX788 (MESH:C000710874), zanidatamab (MESH:C000726995), olaparib (MESH:C531550), 27-hydroxycholesterol (MESH:C076996), Nivolumab (MESH:D000077594), lipid (MESH:D008055), irinotecan (MESH:D000077146), doxorubicin (MESH:D004317), PRI-724 (MESH:C492448), ADP (MESH:D000244), idelalisib (MESH:C552946), capecitabine (MESH:D000069287), mirdametinib (MESH:C506614), Nintedanib (MESH:C530716), 5-FU (MESH:D005472), alpelisib (MESH:C585539), RNS (MESH:D011886)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Fusobacterium nucleatum (species) [taxon 851], Alcaligenes faecalis (species) [taxon 511], Homo sapiens (human, species) [taxon 9606], Fusobacterium mortiferum (species) [taxon 850], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Clostridium butyricum (species) [taxon 1492], Mus musculus (house mouse, species) [taxon 10090], Solobacterium moorei (species) [taxon 102148]
- **Mutations:** BRAFV600E, G13D, G12C, G12V

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12988139/full.md

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Source: https://tomesphere.com/paper/PMC12988139