Journal of Colon And Rectal Cancer

Journal of Colon And Rectal Cancer

Journal of Colon And Rectal Cancer – Aim And Scope

Open Access & Peer-Reviewed

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Aims & Scope

Journal of Colon and Rectal Cancer (JCRC) publishes mechanistic research elucidating the molecular pathophysiology, biomarker discovery, and disease mechanisms underlying colorectal malignancies and related gastrointestinal pathologies.

Molecular Pathogenesis Biomarker Discovery Disease Mechanisms Cellular Pathways Genetic Alterations

Research ScopeTiered Structure

Molecular Pathogenesis

  • Oncogenic signaling pathways in colorectal carcinogenesis
  • Genetic and epigenetic alterations driving tumor initiation
  • Microsatellite instability and DNA mismatch repair mechanisms
  • Chromosomal instability pathways
  • Tumor suppressor gene inactivation mechanisms
  • Proto-oncogene activation and mutation profiles
Typical Fit:

"Elucidating the role of APC/β-catenin pathway dysregulation in adenoma-carcinoma sequence through organoid models and mechanistic validation"

Biomarker Discovery & Validation

  • Molecular biomarkers for disease stratification
  • Circulating tumor DNA and liquid biopsy markers
  • Protein and metabolite signatures in disease progression
  • MicroRNA and non-coding RNA biomarkers
  • Tumor microenvironment biomarkers
  • Predictive and prognostic molecular indicators
Typical Fit:

"Identification and validation of novel serum metabolite panels distinguishing Lynch syndrome-associated from sporadic colorectal cancer through metabolomic profiling"

Tumor Microenvironment Dynamics

  • Immune cell infiltration patterns and mechanisms
  • Stromal-epithelial interactions in tumor progression
  • Angiogenesis and vascular remodeling pathways
  • Extracellular matrix remodeling mechanisms
  • Cancer-associated fibroblast activation
  • Inflammatory signaling in tumorigenesis
Typical Fit:

"Mechanistic analysis of CAF-derived exosomal miRNAs promoting epithelial-mesenchymal transition in colorectal cancer cells"

Inflammatory Bowel Disease Pathophysiology

  • Molecular mechanisms of chronic intestinal inflammation
  • Epithelial barrier dysfunction in IBD
  • Immune dysregulation pathways in Crohn's disease and ulcerative colitis
  • Microbiome-host interactions in IBD pathogenesis
  • IBD-associated colorectal cancer molecular mechanisms
  • Fibrosis and stricture formation pathways
Typical Fit:

"Characterization of NOD2 pathway alterations and downstream inflammatory cascades in Crohn's disease-associated dysplasia"

Secondary Focus AreasCross-Disciplinary

Metastatic Mechanisms

Molecular pathways governing colorectal cancer metastasis to liver, lung, and distant organs; circulating tumor cell biology; metastatic niche formation mechanisms

Hereditary Cancer Syndromes

Molecular characterization of familial adenomatous polyposis (FAP), Lynch syndrome, and other hereditary colorectal cancer syndromes; germline mutation effects on cellular pathways

Therapeutic Resistance Mechanisms

Molecular basis of chemoresistance and targeted therapy resistance; adaptive cellular responses to therapeutic pressure; resistance biomarker identification

Immunological Mechanisms

Immune evasion strategies; checkpoint molecule expression patterns; tumor-infiltrating lymphocyte dysfunction mechanisms; immunosuppressive pathway activation

Metabolic Reprogramming

Altered metabolic pathways in colorectal cancer cells; Warburg effect mechanisms; lipid metabolism dysregulation; metabolic dependencies and vulnerabilities

Stem Cell Biology

Cancer stem cell identification and characterization; stem cell niche dynamics; self-renewal pathway mechanisms; differentiation hierarchy disruption

Emerging Research FrontiersSelective

High-Impact Emerging Areas

Note: Submissions in these areas undergo additional editorial review for mechanistic depth and translational potential. Purely descriptive or correlative studies are discouraged.
Single-cell transcriptomics revealing tumor heterogeneity mechanisms
Spatial transcriptomics mapping tumor microenvironment architecture
Organoid models elucidating patient-specific disease mechanisms
CRISPR-based functional genomics identifying disease drivers
Artificial intelligence for biomarker pattern discovery
Microbiome-metabolome interactions in colorectal pathogenesis
Extracellular vesicle-mediated intercellular communication
Epitranscriptomic modifications in cancer progression
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Article Types & Priorities

Priority 1: Fast-Track Review

Expedited
Original Research Articles Systematic Reviews & Meta-Analyses Methods & Resources Mechanistic Studies

Priority 2: Standard Review

Regular
Short Communications Data Notes Perspectives & Commentaries Technical Notes

Rarely Considered

Selective
Case Reports (only with mechanistic insights) Opinion Pieces (by invitation)

Editorial Standards & Requirements

Reporting Guidelines

  • ARRIVE guidelines for animal studies
  • MIQE guidelines for qPCR experiments
  • REMARK guidelines for biomarker studies
  • PRISMA guidelines for systematic reviews
  • STROBE guidelines for observational studies

Data Transparency

  • Raw data deposition in public repositories
  • Omics data in GEO, ArrayExpress, or SRA
  • Protein data in ProteomeXchange
  • Code availability for computational analyses
  • Material availability statements required

Ethics & Integrity

  • IRB/Ethics committee approval for human samples
  • IACUC approval for animal experiments
  • Informed consent documentation
  • Conflict of interest disclosure
  • Adherence to Helsinki Declaration principles

Preprint & Prior Publication

  • Preprints on bioRxiv/medRxiv accepted
  • Conference abstracts do not preclude submission
  • No prior publication in peer-reviewed journals
  • Preprint DOI must be disclosed at submission
  • Significant revisions from preprint expected
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Decision Metrics

21 Days to First Decision
53% Acceptance Rate
45 Days to Publication
Open Access Model

Ready to Submit Your Research?

If your work elucidates molecular mechanisms, identifies novel biomarkers, or advances mechanistic understanding of colorectal pathophysiology, we want to hear from you.

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