Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

DNA Microarrays02:34

DNA Microarrays

19.8K
Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
19.8K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A simple radioassay for detection of antithyroglobulin autoantibodies.

The Indian journal of medical research·1992
Same author

An immunoradiometric assay for measurement of serum thyroglobulin.

The Indian journal of medical research·1992
Same author

Modification of radiosensitivity by the so-called tissue recovery stimulator. I. Radiosensitizing effects of solcoseryl.

Journal of radiation research·1992
Same author

Postnatal laminar development of cholinergic receptors, protein kinase C and dihydropyridine-sensitive calcium antagonist binding in rat visual cortex. Effect of visual deprivation.

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience·1992
Same author

Cerebral glucose metabolic rates after 30 and 45 minute acquisitions: a comparative study.

Journal of nuclear medicine : official publication, Society of Nuclear Medicine·1992
Same author

Resolution of dihydroxyeicosanoates and of dihydroxyeicosatrienoates by chiral phase chromatography.

Analytical biochemistry·1992
Same journal

Polyfunctional Thiazole/Thiazolidinone Derivatives as a New Class of Heterocyclic Compounds with Novel Mechanisms of Anticancer Activity.

Experimental oncology·2026
Same journal

Metabolic Inhibitors and their Impact on Cancer Cell Migration, Invasion, and Metastasis.

Experimental oncology·2026
Same journal

Changes in Cytokine Profile of Macrophages Induced by Chronic Stress in intact and tumor-bearing rats.

Experimental oncology·2026
Same journal

Integrated Analysis of hsa-miR-26b-5p and hsa-miR-186-5p in Blood Serum and Tumor Tissue Reveals their Prognostic and Predictive Significance in Breast Cancer.

Experimental oncology·2026
Same journal

FNBP1 in Chronic Myeloid Leukemia: Spatial Association with BCR-ABL and Potential Implications for Targeted Therapy.

Experimental oncology·2026
Same journal

Stress-Induced Changes in the Methylation Status of Mmp1 and Mmp8 Genes in Tumor Tissue of Rats with Guerin Carcinoma.

Experimental oncology·2026
See all related articles

Related Experiment Video

Updated: Nov 24, 2025

Author Spotlight: Unveiling Transmembrane Protein Family-Related Markers in Gastric Cancer and Implications for Targeted Therapies
07:47

Author Spotlight: Unveiling Transmembrane Protein Family-Related Markers in Gastric Cancer and Implications for Targeted Therapies

Published on: September 15, 2023

1.9K

Microarray based gene expression profiling of advanced gall bladder cancer.

A Kumar1, R Gupta1, N Mathur1

  • 1Dr. B.R.A., Institute-Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi 110029, India.

Experimental Oncology
|December 28, 2020
PubMed
Summary
This summary is machine-generated.

Gall bladder cancer (GBC) involves complex molecular mechanisms. This study identified differentially expressed genes, including Cdc45 and MCM4, suggesting their oncogenic role and potential as therapeutic targets in advanced GBC.

More Related Videos

Colorectal Cancer Cell Surface Protein Profiling Using an Antibody Microarray and Fluorescence Multiplexing
15:17

Colorectal Cancer Cell Surface Protein Profiling Using an Antibody Microarray and Fluorescence Multiplexing

Published on: September 25, 2011

14.2K
Author Spotlight: Genetic Profiling for Fluorouracil Response in Gastric Cancer
06:21

Author Spotlight: Genetic Profiling for Fluorouracil Response in Gastric Cancer

Published on: May 10, 2024

990

Related Experiment Videos

Last Updated: Nov 24, 2025

Author Spotlight: Unveiling Transmembrane Protein Family-Related Markers in Gastric Cancer and Implications for Targeted Therapies
07:47

Author Spotlight: Unveiling Transmembrane Protein Family-Related Markers in Gastric Cancer and Implications for Targeted Therapies

Published on: September 15, 2023

1.9K
Colorectal Cancer Cell Surface Protein Profiling Using an Antibody Microarray and Fluorescence Multiplexing
15:17

Colorectal Cancer Cell Surface Protein Profiling Using an Antibody Microarray and Fluorescence Multiplexing

Published on: September 25, 2011

14.2K
Author Spotlight: Genetic Profiling for Fluorouracil Response in Gastric Cancer
06:21

Author Spotlight: Genetic Profiling for Fluorouracil Response in Gastric Cancer

Published on: May 10, 2024

990

Area of Science:

  • Oncology
  • Molecular Biology
  • Genomics

Background:

  • Gall bladder cancer (GBC) is aggressive, with unknown molecular drivers.
  • GBC shows predilection for females and specific geographic regions.

Purpose of the Study:

  • To comprehensively analyze differentially expressed genes in advanced GBC versus chronic cholecystitis (CC).
  • To identify potential molecular targets for GBC diagnosis and therapy.

Main Methods:

  • Microarray analysis of 12 advanced GBC and 4 CC fresh tissue specimens.
  • In silico analysis and immunohistochemistry validation of selected genes (TPX2, Cdc45, MCM4).

Main Results:

  • Identified 1307 differentially expressed genes (535 upregulated, 772 downregulated) in advanced GBC vs CC.
  • Key affected pathways include cell cycle, DNA replication, and oxidative stress.
  • Cdc45 and MCM4 proteins showed significant positive association in advanced GBC (p=0.043).

Conclusions:

  • The Cdc45-MCM4 axis is potentially regulated in advanced GBC.
  • Differentially expressed genes like TPX2, Cdc45, and MCM4 may serve as future diagnostic or therapeutic targets.