ReviewDiscover oncology2026
Advancements and innovations in the molecular mechanisms and treatment of colorectal cancer.
Review in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- The distinguished predictive value of CFIm25 in schistosomal and non-schistosomal colorectal cancer.Translational cancer research · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Colorectal cancer (CRC) remains a major global health challenge due to its high incidence and mortality rates. The development and progression of CRC are driven by complex molecular mechanisms involving genetic alterations in proto-oncogenes such as BRAF, PIK3CA, and K-ras, as well as tumor suppressor genes including APC, p53, and PTEN. These genetic changes are further compounded by the dysregulation of key signaling pathways such as Wnt/β-Catenin, PI3K/Akt, and STAT3, which collectively promote tumor cell proliferation, invasion, and metastasis. Additionally, chronic inflammation mediated by pro-inflammatory cytokines like TNF-α, IL-6, and IL-8, along with disruptions in gut microbiota homeostasis, play critical roles in CRC pathogenesis by facilitating immune evasion and tumor progression.In recent years, significant advancements in therapeutic strategies have improved outcomes for CRC patients. Immunotherapy, including immune checkpoint inhibitors, tumor vaccines, and adoptive cell therapy, has shown promising results, particularly in patients with specific molecular profiles. Targeted therapies directed against biomarkers such as EGFR, VEGF, KRAS, and BRAF have also demonstrated efficacy, while complementary approaches like traditional Chinese medicine have gained attention for their potential to enhance treatment outcomes. However, challenges such as tumor heterogeneity, drug resistance, and the complex tumor microenvironment continue to hinder therapeutic success, underscoring the need for further research to overcome these barriers and improve patient survival.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.