Journal of Hematology and Oncology Research

Journal of Hematology and Oncology Research

Journal of Hematology and Oncology Research – Aim And Scope

Open Access & Peer-Reviewed

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Aims & Scope

The Journal of Hematology and Oncology Research (JHOR) publishes high-quality research across the full spectrum of hematology and oncology, including basic, translational, clinical, and diagnostic studies that advance understanding and treatment of blood disorders and cancer.

Hematology Research Oncology Research Translational Studies Clinical Investigations Molecular Pathogenesis
Scope Focus: We welcome studies that advance knowledge in hematology and oncology through mechanistic insights, clinical observations, translational applications, or diagnostic innovation. All submissions should contribute meaningfully to understanding disease biology or improving patient outcomes.

The Journal of Hematology and Oncology Research (JHOR) publishes high-impact research across hematology and oncology, encompassing basic science, translational studies, clinical investigations, and diagnostic innovations. The journal serves as a platform for discoveries that deepen understanding of blood disorders and cancer, improve disease classification, and inform therapeutic development.

We welcome original research on molecular pathophysiology, tumor biology, immune mechanisms, hematopoiesis, and disease modeling, as well as translational and clinical studies that bridge laboratory findings with patient care. Research using patient samples, omics technologies, cellular systems, animal models, and clinical datasets is encouraged, provided it advances scientific or clinical knowledge in the field.

Clinical, pathological, and diagnostic studies are within scope when they provide novel insights into disease mechanisms, identify new therapeutic targets, or demonstrate clinical relevance of biological findings. Case reports are considered when they describe rare presentations, novel therapeutic responses, or unique biological insights.

Article types include original research, reviews, methods and protocols, short communications, data notes, case reports, and commentaries. JHOR serves researchers, clinicians, and scientists in hematology, oncology, translational medicine, and related disciplines.

Core Research Domains

Molecular Oncology

  • Cancer genomics and epigenetic modifications in tumorigenesis
  • Signal transduction pathways driving malignant transformation
  • Tumor microenvironment interactions and cellular crosstalk
  • Cancer stem cell biology and self-renewal mechanisms
  • Molecular basis of metastasis and invasion
  • Oncogene and tumor suppressor gene function
Typical Fit Example: Identification of novel signaling pathways regulating epithelial-mesenchymal transition in breast cancer cells, with validation using CRISPR-Cas9 gene editing and pathway inhibitor studies.

Hematological Pathophysiology

  • Molecular mechanisms of hematopoiesis and lineage commitment
  • Pathogenesis of leukemias and lymphomas at cellular level
  • Genetic and epigenetic drivers of hematologic malignancies
  • Molecular basis of hemolytic anemias and coagulopathies
  • Platelet and leukocyte dysfunction mechanisms
  • Stem cell biology and bone marrow microenvironment
Typical Fit Example: Investigation of JAK2 V617F mutation effects on megakaryocyte differentiation and platelet production in myeloproliferative neoplasms using patient-derived cells and mouse models.

Cancer Immunology

  • Tumor-immune system interactions and immune evasion mechanisms
  • Molecular basis of immune checkpoint regulation
  • T cell exhaustion and dysfunction in tumor microenvironment
  • Antigen presentation and recognition pathways in cancer
  • Innate immune responses to malignant cells
  • Immunosuppressive mechanisms in tumor progression
Typical Fit Example: Molecular characterization of PD-L1 upregulation mechanisms in melanoma cells under hypoxic conditions, including transcriptional regulation and post-translational modifications.

Biomarkers & Molecular Diagnostics

  • Discovery and validation of disease-specific biomarkers
  • Molecular signatures for disease classification and prognosis
  • Circulating tumor markers and liquid biopsy analytes
  • Genetic and proteomic profiling for disease stratification
  • Molecular mechanisms underlying biomarker expression
  • Novel diagnostic targets in hematologic and oncologic diseases
Typical Fit Example: Identification of circulating microRNA signatures associated with acute myeloid leukemia progression, with studies linking miRNA expression to leukemogenesis pathways.

Secondary Focus Areas

Pharmacogenetics & Drug Mechanisms

Molecular mechanisms of drug resistance, pharmacogenomic determinants of treatment response, and cellular pathways mediating chemoresistance in hematologic and oncologic diseases.

Disease Modeling Systems

Development and validation of cellular and animal models recapitulating disease pathophysiology, including patient-derived xenografts, organoids, and genetically engineered models.

Molecular Cytogenetics

Chromosomal abnormalities and structural variants in hematologic malignancies and solid tumors, including mechanisms of chromosomal instability and DNA damage responses.

Tumor Metabolism

Metabolic reprogramming in cancer cells, metabolic dependencies of malignant cells, and metabolic interactions within the tumor microenvironment.

Molecular Mechanisms of Angiogenesis

Vascular development in tumors, pro-angiogenic signaling pathways, and molecular regulators of tumor blood vessel formation and function.

Hereditary Cancer Genetics

Germline mutations predisposing to hematologic and oncologic diseases, molecular mechanisms of inherited cancer syndromes, and genotype-phenotype correlations.

Emerging Research Areas

Encouraged with Scientific Merit

The following areas are actively encouraged when they contribute novel insights to hematology or oncology. Submissions undergo standard editorial review with attention to scientific rigor and relevance.

AI-Driven Molecular Analysis: Machine learning approaches for identifying disease mechanisms, pathway analysis, and molecular pattern recognition in omics datasets.
Single-Cell Mechanistic Studies: Single-cell genomics, transcriptomics, and proteomics revealing cellular heterogeneity and clonal evolution in disease.
Epigenetic Regulation: DNA methylation, histone modifications, and chromatin remodeling mechanisms in hematologic and oncologic pathogenesis.
Extracellular Vesicle Biology: Molecular cargo and signaling mechanisms of exosomes and microvesicles in disease progression and cell-cell communication.
Molecular Imaging Biomarkers: Novel imaging agents and techniques for visualizing disease processes at molecular and cellular levels.
Molecular Mechanisms in Rare Cancers: Pathophysiological mechanisms of uncommon malignancies with unique molecular features.

Article Types & Editorial Priorities

Priority 1

Fast-Track Review

Priority 2

Standard Review

Occasionally Accepted

Selective Acceptance

Editorial Standards & Requirements

Reporting Guidelines

  • ARRIVE guidelines for animal studies
  • MIQE for qPCR experiments
  • PRISMA for systematic reviews
  • REMARK for biomarker studies
  • STARD for diagnostic accuracy

Data Transparency

  • Raw data deposition in public repositories
  • Genomic data in GEO or ArrayExpress
  • Proteomic data in PRIDE or ProteomeXchange
  • Code availability for computational analyses
  • Materials and reagent sharing statements

Ethics & Integrity

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

Preprint Policy

  • Preprints on bioRxiv, medRxiv accepted
  • Must disclose preprint DOI at submission
  • Preprint posting does not affect consideration
  • Final version must acknowledge preprint
  • Preprint servers must be non-commercial

Editorial Decision Metrics

21 days Average Time to First Decision
32% Acceptance Rate
45 days Average Time to Publication
Open Access Model (APC-based)