Issues
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Cover Image
Cover Image
Albumin-bound/conjugated chemotherapies such as nab-paclitaxel (Abraxane) are a class of chemotherapies that have shown improvements over conventional chemotherapy in certain tumor types, resulting in reduced toxicity and/or increased efficacy. The improved targeting to tumor cells is thought to be in part due to an enhanced permeability and retention effect within tumors, but no useful molecular biomarkers exist to predict efficacy to this class of drugs. Caveolae are flask-shaped invaginations of the plasma membrane that appear important for albumin uptake, and caveolin-1 is the protein required for caveolae formation. Using immunofluorescence, it was found that the degree of caveolin-1 expression dictates uptake of nab-paclitaxel, as visualized by immunofluorescence for albumin (green) in DAPI-stained (blue) tumor cells. For details, see article by Chatterjee and colleagues on page 5925. - PDF Icon PDF LinkTable of Contents
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Cancer Research
Table of Contents
Focus on Computer Resources
The Cancer Genomics Cloud: Collaborative, Reproducible, and Democratized—A New Paradigm in Large-Scale Computational Research
The ISB Cancer Genomics Cloud: A Flexible Cloud-Based Platform for Cancer Genomics Research
Developing Cancer Informatics Applications and Tools Using the NCI Genomic Data Commons API
Software for the Integration of Multiomics Experiments in Bioconductor
An Accessible Proteogenomics Informatics Resource for Cancer Researchers
PDX-MI: Minimal Information for Patient-Derived Tumor Xenograft Models
SlicerDMRI: Open Source Diffusion MRI Software for Brain Cancer Research
TumorMap: Exploring the Molecular Similarities of Cancer Samples in an Interactive Portal
“Personalized Cancer Therapy”: A Publicly Available Precision Oncology Resource
Breaking Advances
Reviews
A Collaborative Model for Accelerating the Discovery and Translation of Cancer Therapies
Perspective
Meeting Report
Priority Report
Discovery of Human-Similar Gene Fusions in Canine Cancers
Molecular and Cellular Pathobiology
miR-193b–Regulated Signaling Networks Serve as Tumor Suppressors in Liposarcoma and Promote Adipogenesis in Adipose-Derived Stem Cells
Upregulation of Cystathionine-β-Synthase in Colonic Epithelia Reprograms Metabolism and Promotes Carcinogenesis
YAP Suppresses Lung Squamous Cell Carcinoma Progression via Deregulation of the DNp63–GPX2 Axis and ROS Accumulation
Genetic Dissociation of Glycolysis and the TCA Cycle Affects Neither Normal nor Neoplastic Proliferation
Tumor and Stem Cell Biology
Exosomes from Glioma-Associated Mesenchymal Stem Cells Increase the Tumorigenicity of Glioma Stem-like Cells via Transfer of miR-1587
ANGPTL1 Interacts with Integrin α1β1 to Suppress HCC Angiogenesis and Metastasis by Inhibiting JAK2/STAT3 Signaling
These results suggest a secreted tumor suppressor has the potential to be developed as a novel prognostic biomarker and novel therapeutic target in liver cancer.
Lysyl Oxidase–like Protein LOXL2 Promotes Lung Metastasis of Breast Cancer
Conditional transgenic mouse models establish a new role for an ECM regulator in metastatic invasion that is independent of its canonical function in ECM remodeling.
Novel SEC61G–EGFR Fusion Gene in Pediatric Ependymomas Discovered by Clonal Expansion of Stem Cells in Absence of Exogenous Mitogens
ATG5 Mediates a Positive Feedback Loop between Wnt Signaling and Autophagy in Melanoma
FSTL1 Promotes Metastasis and Chemoresistance in Esophageal Squamous Cell Carcinoma through NFκB–BMP Signaling Cross-talk
KDM4 Inhibition Targets Breast Cancer Stem–like Cells
Therapeutics, Targets, and Chemical Biology
MCT1 Inhibitor AZD3965 Increases Mitochondrial Metabolism, Facilitating Combination Therapy and Noninvasive Magnetic Resonance Spectroscopy
Microenvironment and Immunology
Gemcitabine-Induced TIMP1 Attenuates Therapy Response and Promotes Tumor Growth and Liver Metastasis in Pancreatic Cancer
Enhanced Acid Sphingomyelinase Activity Drives Immune Evasion and Tumor Growth in Non–Small Cell Lung Carcinoma
Transplantation of iPS-Derived Tumor Cells with a Homozygous MHC Haplotype Induces GRP94 Antibody Production in MHC-Matched Macaques
Integrated Systems and Technologies
Prevention and Epidemiology
Letter to the Editor
Cross-Cancer Analysis Reveals Novel Pleiotropic Associations—Response
Corrections
Journal Archive
Cancer Research
(1941-Present; volumes 1-current)Published twice monthly since 1987. From 1941-1986, published monthly.
(ISSN 0008-5472)
The American Journal of Cancer
(1931-1940; volumes 15-40)Published quarterly in 1931, bimonthly in 1932, and monthly from 1933 to 1940. The journal changed title to Cancer Research in 1941.
(ISSN 0099-7374)
The Journal of Cancer Research
(1916-1930); volumes 1-14)Published quarterly from 1916 through 1930 (publication was suspended from November 1922 to March 1924). The journal changed title to The American Journal of Cancer in 1931.
(ISSN 0099-7013)
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