Target landscape
Open Targets · retrieved 2026-09-30 · weekly12 genes recurrently implicated in colorectal cancer, triaged for whether anything can actually be aimed at them. The zeros are the informative rows.
Of 12 recurrently implicated genes, 8 carry any drug at all. That is a statement about these 12 gene targets, not about the disease: Colorectal cancer does have labelled therapy — 15 drugs, listed in the next section.
Two different questions
The table below asks what can be aimed at 12 recurrently implicated genes. That is narrower than what is approved for the disease, and narrower again than what colorectal cancer is actually treated with, which includes agents approved under broader indications. All three are on this page and they are kept apart deliberately.
| Gene | Drugs | Approval, and whether it reached this disease | Open Targets tractabilitycomputed from protein features and literature — a signal that a modality is worth trying, not evidence that it works | Cell therapy here |
|---|---|---|---|---|
| APC across cancers → | 0 | No drug— | antibody, protein degrader, small molecule | — |
| KRAS across cancers → | 3 | 2 approvedAdagrasib, SotorasibApproved in colorectal cancer: Adagrasib, Sotorasib.12 active of 18 colorectal cancer trials | antibody, protein degrader, small molecule | — |
| TP53 across cancers → | 8 | Phase 3Alrizomadlin, Cenersen, Contusugene Ladenovec, Eprenetapopt, Idasanutlin, Navtemadlin, Siremadlin, Teprasiran3 trials, none active | other clinical modality, protein degrader, small molecule | — |
| SMAD4 across cancers → | 0 | No drug— | protein degrader, small molecule | — |
| BRAF across cancers → | 16 | 3 approvedDabrafenib, Sorafenib, TovorafenibApproved in metastatic melanoma, low grade glioma, renal cell carcinoma and 1 other indications. No colorectal cancer indication appears on these drugs’ labels.72 active of 226 colorectal cancer trials | antibody, protein degrader, small molecule | — |
| EGFR across cancers → | 72 | 15 approvedAfatinib, Aumolertinib, Brigatinib, Cetuximab Sarotalocan, Dacomitinib, Erlotinib, Icotinib, Lapatinib, Lazertinib, Mobocertinib, Neratinib, Nimotuzumab, Olmutinib, Osimertinib, RociletinibApproved in non-small cell lung carcinoma, anaplastic large cell lymphoma, head and neck cancer and 3 other indications. No colorectal cancer indication appears on these drugs’ labels.100 active of 460 colorectal cancer trials | antibody, other clinical modality, protein degrader, small molecule | 1 active of 3 trials |
| ERBB2 across cancers → | 43 | 10 approvedAfatinib, Dacomitinib, Lapatinib, Margetuximab, Masoprocol, Neratinib, Trastuzumab Duocarmazine, Tucatinib, Zanidatamab, ZenocutuzumabApproved in colorectal cancer: Tucatinib.66 active of 144 colorectal cancer trials | antibody, other clinical modality, protein degrader, small molecule | 0 active of 1 trial |
| PIK3CA across cancers → | 31 | 2 approvedCopanlisib, InavolisibApproved in follicular lymphoma, non-Hodgkin lymphoma, neoplasm of mature B-cells and 1 other indications. No colorectal cancer indication appears on these drugs’ labels.5 active of 21 colorectal cancer trials | antibody, protein degrader, small molecule | — |
| MLH1 across cancers → | 0 | No drug— | protein degrader, small molecule | — |
| MSH2 across cancers → | 0 | No drug— | protein degrader, small molecule | — |
| NTRK1 across cancers → | 16 | 4 approvedEntrectinib, Larotrectinib, Lestaurtinib, RepotrectinibApproved in non-small cell lung carcinoma, metastasis, acute myeloid leukemia by FAB classification. No colorectal cancer indication appears on these drugs’ labels.45 active of 149 colorectal cancer trials | antibody, other clinical modality, protein degrader, small molecule | — |
| CEACAM5 across cancers → | 5 | Phase 3Arcitumomab, Labetuzumab, Labetuzumab Govitecan, Medi-565, Tusamitamab Ravtansine9 trials, none active | antibody, other clinical modality, small molecule | 8 active of 18 trials |
Dataset evidence counts studies in the 2072-study ranked set whose title or abstract names the gene; the bar is scaled to KRAS. Sources: Open Targets Platform and NCBI GEO, retrieved 2026-09-30. Clinical stage is the highest reached for any indication — see the per-drug indications noted in each row. Target-prioritisation reference only; not clinical or prescribing guidance.
What is actually approved here
openFDA drug labels · weekly15 drugs carry an FDA label naming colorectal cancer: Adagrasib, Bevacizumab, Cetuximab, Encorafenib, Fruquintinib, Ipilimumab, Nivolumab, Panitumumab, Pembrolizumab, Ramucirumab, Regorafenib, Sotorasib, Trifluridine And Tipiracil, Tucatinib, Ziv-Aflibercept. Separately, 29 of the drugs returned for the genes in the table above are approved only for other diseases and reach colorectal cancer through trials, not through their labels.
Every label that names colorectal cancer
| Drug | Role | What the label says |
|---|---|---|
| AdagrasibKRAZATI | Labelled here | Colorectal cancer (CRC)* • In combination with cetuximab, for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic CRC, as determined by an FDA-approved test, who have received prior treatment with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy. |
| BevacizumabALYMSYS, Avastin, JOBEVNE | Labelled here | Metastatic Colorectal Cancer MVASI, in combination with intravenous fluorouracil-based chemotherapy, is indicated for the first- or second-line treatment of patients with metastatic colorectal cancer (mCRC). |
| CetuximabERBITUX | Labelled here | ( 1.1 , 14.1 ) Colorectal Cancer K-Ras wild-type, EGFR-expressing, metastatic colorectal cancer as determined by an FDA-approved test in combination with FOLFIRI for first-line treatment, in combination with irinotecan in patients who are refractory to irinotecan-based chemotherapy, as a single-agent in patients who have failed oxaliplatin- and irinotecan-based chemotherapy or who are intoleran... |
| EncorafenibBRAFTOVI | Labelled here | ( 1.1 , 2.1 ) Colorectal Cancer (CRC) • in combination with cetuximab and fluorouracil-based chemotherapy, for the treatment of adult patients with metastatic colorectal cancer (mCRC) with a BRAF V600E mutation, as detected by an FDA‑authorized test. |
| FruquintinibFruzaqla | Labelled here | FRUZAQLA is a kinase inhibitor indicated for the treatment of adult patients with metastatic colorectal cancer (mCRC) who have been previously treated with fluoropyrimidine‑, oxaliplatin‑, and irinotecan‑based chemotherapy, an anti‑VEGF therapy, and, if RAS wild‑type and medically appropriate, an anti-EGFR therapy. |
| IpilimumabYERVOY | Labelled here | Colorectal Cancer • Treatment of adults and pediatric patients 12 years and older with unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) colorectal cancer (CRC) as determined by an FDA-authorized test in combination with nivolumab. |
| NivolumabOPDIVO, OPDIVO QVANTIG | Labelled here | Colorectal Cancer • adult and pediatric (12 years and older) patients with unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) colorectal cancer (CRC) in combination with ipilimumab. |
| PanitumumabVectibix | Labelled here | Metastatic Colorectal Cancer (mCRC) RAS Wild-Type mCRC Vectibix is indicated for the treatment of adult patients with wild-type RAS (defined as wild-type in both KRAS and NRAS as determined by an FDA-approved test) metastatic colorectal cancer (mCRC) [see Dosage and Administration |
| PembrolizumabKEYTRUDA, KEYTRUDA QLEX | Labelled here | Microsatellite Instability-High or Mismatch Repair Deficient Colorectal Cancer KEYTRUDA is indicated for the treatment of patients with unresectable or metastatic MSI-H or dMMR colorectal cancer (CRC) as determined by an FDA-authorized test [see Dosage and Administration |
| RamucirumabCYRAMZA | Labelled here | Colorectal Cancer CYRAMZA, in combination with FOLFIRI (irinotecan, folinic acid, and fluorouracil), is indicated for the treatment of adults with metastatic colorectal cancer (mCRC) with disease progression on or after prior therapy with bevacizumab, oxaliplatin, and a fluoropyrimidine. |
| RegorafenibStivarga | Labelled here | Colorectal Cancer STIVARGA is indicated for the treatment of adult patients with metastatic colorectal cancer (CRC) who have been previously treated with fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapy, an anti-VEGF therapy, and, if RAS wild-type, an anti-EGFR therapy. |
| SotorasibLUMAKRAS | Labelled here | KRAS G12C-mutated Metastatic Colorectal Cancer (mCRC) In combination with panitumumab, for the treatment of adult patients with KRAS G12C-mutated mCRC as determined by an FDA approved-test, who have received prior fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapy. |
| Trifluridine And TipiracilLONSURF | Labelled here | Metastatic Colorectal Cancer LONSURF, as a single agent or in combination with bevacizumab, is indicated for the treatment of adult patients with metastatic colorectal cancer previously treated with fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapy, an anti-VEGF biological therapy, and if RAS wild-type, an anti-EGFR therapy. |
| TucatinibTUKYSA | Labelled here | Unresectable or Metastatic Colorectal Cancer TUKYSA is indicated in combination with trastuzumab for the treatment of adult patients with RAS wild-type, HER2-positive unresectable or metastatic colorectal cancer that has progressed following treatment with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy. |
| Ziv-AfliberceptZALTRAP | Labelled here | ZALTRAP, in combination with fluorouracil, leucovorin, irinotecan-(FOLFIRI), is indicated for the treatment of patients with metastatic colorectal cancer (mCRC) that is resistant to or has progressed following an oxaliplatin-containing regimen. |
| CapecitabineCAPECITABINE, Capecitabine, Capecitabine 150mg | Backbone | Colorectal Cancer XELODA is indicated as a single agent for adjuvant treatment in patients with Dukes' C colon cancer who have undergone complete resection of the primary tumor when treatment with fluoropyrimidine therapy alone is preferred. |
| IrinotecanCamptosar, IRINOTECAN HYDROCHLORIDE, Irinotecan Hydrochloride | Backbone | ( 1 ) Patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following initial fluorouracil-based therapy. |
| Irinotecan HydrochloideIrinotecan hydrochloide, Irinotecan hydrochloride | Backbone | ( 1 ) Patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following initial fluorouracil-based therapy. |
| OxaliplatinOxaliplatin, USP, oxaliplatin | Backbone | (1) treatment of advanced colorectal cancer. |
| Leucovorin CalciumLEUCOVORIN CALCIUM, Leucovorin Calcium, Leucovorin calcium | Supportive | Treatment of patients with metastatic colorectal cancer in combination with 5-fluorouracil. |
| LevoleucovorinKHAPZORY, LEVOLEUCOVORIN, LEVOLEUCOVORIN CALCIUM | Supportive | ( 1 ) Treatment of adults with metastatic colorectal cancer in combination with fluorouracil. |
| Levoleucovorin CalciumLevoleucovorin | Supportive | ( 1 ) Treatment of adults with metastatic colorectal cancer in combination with fluorouracil. |
113 labels carry a positive indication naming the disease under indications_and_usage:"colorectal cancer" OR indications_and_usage:"colon cancer" OR indications_and_usage:"rectal cancer" OR indications_and_usage:"carcinoma of the colon or rectum" OR indications_and_usage:"colorectal carcinoma"; they collapse to 22 distinct molecules once salt forms, biosimilars and co-formulated hyaluronidase are merged. Supportive agents (Leucovorin Calcium, Levoleucovorin, Levoleucovorin Calcium) are given in the disease but do not act on it. Source: openFDA drug label API (api.fda.gov/drug/label.json), retrieved 2026-09-18. Labels change; this reflects the current label text, not the approval history. Not prescribing guidance.
Labels that name colorectal cancer without indicating for it
A label can name a disease under Limitations of Use, in a contraindication or as a risk. These were read and are not counted above.
| Drug | Why not | What the label says |
|---|---|---|
| DabrafenibTafinlar | Excluded by label | Limitations of Use : TAFINLAR is not indicated for treatment of patients with colorectal cancer because of known intrinsic resistance to BRAF inhibition. |
| TrametinibMekinist | Excluded by label | Limitations of Use : MEKINIST is not indicated for treatment of patients with colorectal cancer because of known intrinsic resistance to BRAF inhibition. |
Cell therapy against CEA
ClinicalTrials.gov · retrieved 2026-09-18 · weeklyCEA is the busiest cell-therapy target among those this briefing searched in colorectal cancer: 18 registered trials naming it, 8 still active, 2 withdrawn before enrolling anyone. It has no gene entry of its own and is reached through CEACAM5: the surface glycoprotein CEACAM5 encodes, the CEA of the blood test.
| Trial | Phase | Status | Title | Last update |
|---|---|---|---|---|
| NCT05240950 | 1 | Recruiting | Anti-CEA CAR-T Cells to Treat Colorectal Liver Metastases | 2022-03-11 |
| NCT06043466 | 1 | Recruiting | A Clinical Trial Targeting CEA Chimeric Antigen Receptor T (CAR-T) for CEA Positive Advanced Malignant Solid Tumors | 2023-09-21 |
| NCT06010862 | 1 | Recruiting | Clinical Study of CEA-targeted CAR-T Therapy for CEA-positive Advanced/Metastatic Malignant Solid Tumors | 2023-11-08 |
| NCT06126406 | 1 | Recruiting | Clinical Study of CEA Targeting Chimeric Antigen Receptor T Lymphocytes(CAR-T) for CEA Positive Advanced Malignant Solid Tumors | 2023-11-13 |
| NCT07179692 | 1 | Recruiting | CEA-Targeted CAR-T Therapy in CEA-Positive Advanced Solid Tumors | 2025-10-02 |
| NCT07247396 | 1 | Recruiting | CEA CAR-T Therapy After Cytoreduction in Colorectal Cancer Patients With Peritoneal Metastases | 2025-11-25 |
| NCT06821048 | 1 | Recruiting | Study of CEA Targeting CAR-T (PTC13) in the Treatment of CEA-Positive Advanced Malignant Solid Tumors | 2026-01-23 |
| NCT05736731 | 1/2 | Active | A Study to Evaluate the Safety and Efficacy of A2B530, a Logic-gated CAR T, in Participants With Solid Tumors That Express CEA and Have Lost HLA-A*02 Expression | 2025-04-25 |
| NCT01723306 | 2 | Suspended | Phase II/Pilot Study of 2nd Generation Anti-CEA Designer T Cells in Adenocarcinomas | 2016-06-14 |
| NCT02349724 | 1 | Unknown | A Clinical Research of CAR T Cells Targeting CEA Positive Cancer | 2017-04-25 |
10 of 18 shown, most recently active first. Other targets searched: NKG2D (7), PD-1 (6), EGFR (3), MUC1 (3), GUCY2C (1), HER2 (1), TROP2 (1), LGR5 (1). Source: ClinicalTrials.gov API v2, retrieved 2026-09-18. A trial counts here when its registered conditions name colorectal cancer or a tumour-agnostic basket, its title names an administered cell product, and the title names this target: a HER2 CAR-T trial that adds a PD-1 antibody is a HER2 trial. A trial stating only a product code is missed.
Research momentum
PubMed MeSH · monthlyEvery term below is a share of the colorectal cancer literature, not a count, because the field itself grew: 2015–2018 (n=6,000) against 2021–2025 (n=6,000). A topic whose papers doubled while the field doubled has not risen.
These are sample shares. The two windows hold 32,289 and 48,775 papers; MeSH terms were read from an evenly spaced sample of 6,000 and 6,000 of them, taken across the whole window rather than from its most recent papers. Percentages carry sampling error of roughly a percentage point and small differences between two terms are not meaningful.
Rising, with a real baseline
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Deep Learning | 0.08% | 1.67% | 20.0× | 100 papers |
| Artificial Intelligence | 0.08% | 1.42% | 17.0× | 85 papers |
| Machine Learning | 0.22% | 2.33% | 10.77× | 140 papers |
| Drugs, Chinese Herbal | 0.12% | 0.92% | 7.86× | 55 papers |
| Molecular Docking Simulation | 0.23% | 1.63% | 7.0× | 98 papers |
| Tumor Microenvironment | 1.35% | 8.4% | 6.22× | 504 papers |
| Probiotics | 0.13% | 0.82% | 6.12× | 49 papers |
| Lipid Metabolism | 0.1% | 0.53% | 5.33× | 32 papers |
| Diagnosis, Computer-Assisted | 0.12% | 0.6% | 5.14× | 36 papers |
| Glycolysis | 0.2% | 0.9% | 4.5× | 54 papers |
Cooling
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Survival Analysis | 4.17% | 0.32% | 0.08× | 19 papers |
| Multivariate Analysis | 1.88% | 0.25% | 0.13× | 15 papers |
| Cell Cycle | 1.28% | 0.23% | 0.18× | 14 papers |
| Biopsy | 1.27% | 0.25% | 0.2× | 15 papers |
| Tumor Burden | 2.05% | 0.45% | 0.22× | 27 papers |
| Down-Regulation | 2.47% | 0.53% | 0.22× | 32 papers |
Biggest topics now
| MeSH term | 2015–18 | 2021–25 | Change | Share now |
|---|---|---|---|---|
| Prognosis | 15.18% | 15.27% | 1.01× | 916 papers |
| Gene Expression Regulation, Neoplastic | 12.02% | 14.43% | 1.2× | 866 papers |
| Rectal Neoplasms | 15.33% | 13.98% | 0.91× | 839 papers |
| Colonic Neoplasms | 21.22% | 13.42% | 0.63× | 805 papers |
| Biomarkers, Tumor | 10.68% | 12.42% | 1.16× | 745 papers |
| Cell Proliferation | 11.02% | 11.27% | 1.02× | 676 papers |
| Treatment Outcome | 12.97% | 9.55% | 0.74× | 573 papers |
| Tumor Microenvironment | 1.35% | 8.4% | 6.22× | 504 papers |
| Early Detection of Cancer | 7.3% | 7.87% | 1.08× | 472 papers |
| Risk Factors | 7.83% | 7.68% | 0.98× | 461 papers |
Publication mix
| Type | 2015–18 | 2021–25 |
|---|---|---|
| Clinical Trial | 0.0% | 0.1% |
| Randomized Controlled Trial | 3.1% | 3.4% |
| Review | 7.4% | 8.5% |
| Meta-Analysis | 2.6% | 3.1% |
| Case Reports | 0.0% | 3.5% |
Query: Colorectal Neoplasms[MeSH Major Topic] NOT ("Anus Neoplasms"[MeSH] OR "Neuroendocrine Tumors"[MeSH] OR "Appendiceal Neoplasms"[MeSH]). Terms need at least 12 papers in the recent window and, in the rising table, at least 5 in the earlier one — a term going from 1 paper to 12 is a large fold change and no evidence of anything. Ubiquitous descriptors (Humans, Animals, age bands) and the disease’s own term are dropped. Windows are read whole where they fit and sampled where they do not; the totals and the sample sizes are both in the JSON beside this page. Source: PubMed MeSH, retrieved 2026-09-12.
Disease burden
What the public sources count, and how closely each category matches this disease. The same figures for every disease on the site are on one table.
| Measure | Value | Match | What it counts |
|---|---|---|---|
| New cases each year | 158,850 cases/year | direct | 2026 SEER Cancer Stat Facts, Colorectal Cancer, retrieved 2026-09-12 |
| Deaths each year | 55,230 deaths/year | direct | 2026 SEER Cancer Stat Facts, Colorectal Cancer, retrieved 2026-09-12 |
| Incidence rate | 37.6 cases per 100,000 per year | direct | 2019-2023 SEER Cancer Stat Facts, Colorectal Cancer, retrieved 2026-09-12 |
| Death rate | 12.7 deaths per 100,000 per year | direct | 2020-2024 SEER Cancer Stat Facts, Colorectal Cancer, retrieved 2026-09-12 |
| People living with it | 1,478,528 people living with the disease | direct | 2023 SEER Cancer Stat Facts, Colorectal Cancer, retrieved 2026-09-12 |
| Median age at diagnosis | 66.0 years | direct | 2019-2023 SEER Cancer Stat Facts, Colorectal Cancer, retrieved 2026-09-12 |
| median age at death | 72 years | direct | 2020-2024 SEER Cancer Stat Facts, Colorectal Cancer, retrieved 2026-09-12 |
| Five-year relative survival | 65.4% | direct | 2016-2022 SEER Cancer Stat Facts, Colorectal Cancer, retrieved 2026-09-12 |
Years of life lost (proxy)
4.3 years per case, 681,530 a year, from survival and age at diagnosis rather than from a death count. derived proxy Not the WHO/GBD measure, which uses age at death and a life table; comparable across these briefings, not with published YLL figures. What this costs to fund is in Funding.
3 assumptions behind this estimate
- Five-year relative survival stands in for cure; a death after five years is not counted.
- The median age at diagnosis stands in for the whole age distribution.
- Life expectancy at birth (78.4 years) is the reference, rather than remaining expectancy at the age of death from a life table.
- Each assumption moves the result by more than the difference between the two diseases currently on this site, so this figure separates a disease from one ten times its size, not from a close neighbour.
Funding
NIH RePORTER · quarterlyNIH obligations naming colorectal cancer, after removing the 9,685 records across all years that matched the search but are about something else. That filter is not cosmetic: without it this section reports another field’s funding as this disease’s.
NIH obligations by fiscal year
| Year | Obligations | Awards | Distinct projects | Dropped as off-topic |
|---|---|---|---|---|
| FY2013 | $150.7M | 387 | 326 | 609 |
| FY2014 | $129.1M | 348 | 299 | 624 |
| FY2015 | $134.2M | 375 | 313 | 652 |
| FY2016 | $139.0M | 340 | 311 | 650 |
| FY2017 | $147.5M | 343 | 314 | 636 |
| FY2018 | $198.2M | 413 | 367 | 852 |
| FY2019 | $161.4M | 416 | 367 | 756 |
| FY2020 | $176.0M | 423 | 373 | 805 |
| FY2021 | $189.1M | 457 | 404 | 833 |
| FY2022 | $200.6M | 468 | 417 | 853 |
| FY2023 | $198.0M | 447 | 388 | 845 |
| FY2024 | $190.9M | 446 | 386 | 833 |
| FY2025 | $211.7M | 417 | 370 | 737 |
Where FY2025 money went
| Institution | Obligations | Awards |
|---|---|---|
| Fred Hutchinson Cancer Center | $14.1M | 25 |
| Vanderbilt University Medical Center | $10.3M | 14 |
| University Of Tx Md Anderson Can Ctr | $8.3M | 12 |
| University Of Michigan At Ann Arbor | $8.2M | 11 |
| Weill Medical Coll Of Cornell Univ | $6.5M | 12 |
| University Of Southern California | $6.0M | 0 |
| Division Of Basic Sciences - Nci | $5.4M | 0 |
| Massachusetts General Hospital | $5.3M | 11 |
| Utah State Higher Education System--University Of Utah | $4.9M | 11 |
| Washington University | $4.5M | 10 |
Text search colorectal cancer over project title, terms and abstract, per fiscal year. Awards are individual funding actions; distinct projects collapse them by core project number, so a multi-year grant counts once. The most recent year may be incomplete. Source: NIH RePORTER, retrieved 2026-09-19.
What that buys
Against 681,530 years of life lost a year, FY2025 obligations are $311 per life-year — $1,333 per case. The estimate and its assumptions are in Disease burden.
Who funds it, FY2025
The total says how much. These say who from, through what kind of award, and to whom — which a dollar figure cannot.
NIH institutes
Projects by administering institute. The rows above are the top 10 and account for 415 of 417.
Award mechanisms
R01 is an investigator-initiated grant; ZIA is NIH intramural, meaning the work happens inside NIH rather than being funded outside it. The rows above are the top 15 and account for 364 of 417.
Where it lands
Share of $211.7M in FY2025. The top three hold 15%.
Public datasets, ranked
NCBI GEO + Europe PMC + iCite · weekly5,232 human GEO series match colorectal cancer. Keyword relevance cannot tell a 2,503-sample patient cohort from a six-well cell-line experiment, so this ranking scores four things GEO does not expose: how often the accession is named in full-text papers, field-normalised citation impact, clinical annotation, and cohort type.
Composition of the 2072-study ranked set
Established
high reuse, older| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE14333 | Expression data from 290 primary colorectal cancers2010 · array | 290 | 611 | 6.9 | patient cohortAPT 0.75survivalstage363 cites |
| GSE81861 | Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors2017 · single-cell | 1,220 | 113 | 23.8 | patient cohortAPT 0.75survival841 cites |
| GSE17538 | Experimentally Derived Metastasis Gene Expression Profile Predicts Recurrence and Death in Colon Cancer Patients2009 · array | 244 | 984 | 12.7 | patient cohortAPT 0.75survival615 cites |
| GSE178341 | A Single Cell Atlas of MMRd and MMRp Colorectal Cancer2021 · spatial | 181 | 187 | 32.7 | patient cohortAPT 0.75710 cites |
| GSE132465 | Single cell 3' RNA sequencing of 23 Korean colorectal cancer patients2020 · single-cell | 33 | 364 | 23.8 | patient cohortAPT 0.75668 cites |
| GSE41258 | Expression data from colorectal cancer patients2012 · array | 390 | 478 | 6.2 | patient cohortAPT 0.75324 cites |
| GSE146771 | Single-Cell Analyses Inform Mechanisms of Myeloid-Targeted therapies in colon cancer2020 · single-cell | 20 | 213 | 48.0 | patient cohortAPT 0.751,275 cites |
| GSE40967 | Gene expression Classification of Colon Cancer defines six molecular subtypes with distinct clinical, molecular and survival characteristics2013 · array | 1,048 | 1,738 | 30.4 | APT 0.95survival1,169 cites |
Recent
2022 onward, by score| Accession | Study | Samples | MentionsEurope PMC | RCR | Evidence |
|---|---|---|---|---|---|
| GSE205506 | Remodeling of the Immune and Stromal Cell Compartment by PD-1 Blockade in Mismatch Repair-Deficient Colorectal Cancer2023 · single-cell | 40 | 76 | 23.3 | patient cohortAPT 0.75molecularPD-1318 cites |
| GSE236581 | Spatiotemporal single-cell analysis decodes cellular dynamics underlying different responses to immunotherapy in Colorectal Cancer2024 · single-cell | 169 | 50 | 15.3 | patient cohortAPT 0.75molecularPD-1168 cites |
| GSE225857 | Single-cell and spatial transcriptome analysis reveals the cellular heterogeneity of liver metastatic colorectal cancer2023 · single-cell | 8 | 75 | 16.8 | patient cohortAPT 0.75survival218 cites |
| GSE200997 | Refining Colorectal Cancer Classification and Clinical Stratification Through a Single-Cell Atlas2022 · single-cell | 23 | 98 | 12.1 | patient cohortAPT 0.75194 cites |
| GSE164522 | Single-cell analyses reveal phenotypic linkage between colorectal cancer and liver metastasis2022 · single-cell | 17 | 33 | 22.2 | patient cohortAPT 0.75372 cites |
| GSE245552 | Th17 cells secrete TWEAK to trigger epithelial-mesenchymal transition and promote colorectal cancer liver metastasis (scRNA-seq)2024 · single-cell | 39 | 20 | 8.2 | patient cohortAPT 0.75survival70 cites |
Sources: NCBI GEO + Europe PMC + iCite, retrieved 2026-09-19. SubSeries are collapsed to one row per study by linked PMID. Of 5,101 series retrieved, 96 were dropped by the profile’s exclusion rules and 2,473 named the disease only in passing. The ranked set is a relevance-ranked sample, not a census, so the composition figures describe the sample only.
Where the gaps are
Derived from the sections above · recomputed on every refreshEach card below is a disagreement between two of the tables on this page — a drug that exists but was never tried here, a target that looks tested and was not, a gene with no drug whose product has a busy clinical programme. They are computed from the same facts as the tables, so they cannot contradict them.
APC
Open Targets lists no drug against it and no trial in colorectal cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.
SMAD4
Open Targets lists no drug against it and no trial in colorectal cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.
MLH1
Open Targets lists no drug against it and no trial in colorectal cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.
MSH2
Open Targets lists no drug against it and no trial in colorectal cancer names it. A bounded negative: the sources and search terms are in the JSON beside this page.
CEACAM5
18 cell-therapy trials against CEA, 8 active, and no approved product. The clinical activity is real and none of it has reached a label.
How a machine reads this page
StaticThis page is written to be quoted correctly by a model as much as read by a person. The same facts are available as JSON at the sibling URL below, which is what to cite. The cross-disease layer — burden, genes, drugs and antigens across every briefing — is described at /disease/api.json.
Fully server-rendered
Every figure is in the HTML at first byte. No JavaScript runs, no figure is fetched after load, and nothing on this page requires a renderer to see.
Every number carries a source
Each section names the API it came from and the date it was retrieved: Open Targets (2026-09-30), ClinicalTrials.gov (2026-09-18), openFDA (2026-09-18), NCBI GEO (2026-09-19), PubMed (2026-09-12), NIH RePORTER (2026-09-19).
Negatives stated explicitly
Where the searches find nothing for colorectal cancer — no drug, no trial, no approval — the page says so in those words rather than omitting the row, and names the source searched. An absent row is unquotable; a bounded negative is the finding.
Denominators, not just percentages
Every share is printed with the count and the total it came from, so a figure can be checked rather than taken.
The filters are published
4 exclusion patterns are applied to free text before anything is ranked, because HCT116, HT-29 and Caco-2, with MC38 and CT26 is used as a model system in DNA-damage and cell-cycle biology (HCT116), intestinal barrier and drug absorption (Caco-2), syngeneic tumour immunology (MC38, CT26). What was removed and why is stated in each section rather than silently applied.
{
"disease": "Colorectal cancer",
"mesh": "Colorectal Neoplasms",
"facts": "https://usebiotransfer.org/disease/colorectal-cancer.json",
"methods": "https://usebiotransfer.org/methods/",
"all_diseases": "https://usebiotransfer.org/disease/api.json",
"note": "Every figure on the page is in that JSON with its source and retrieval date. Quote from it rather than from the HTML."
}