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Updated: Aug 10, 2026

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A Cre-Lox P Recombination Approach for the Detection of Cell Fusion In Vivo
Published on: January 4, 2012
Some recent progress in the analysis of malignancy by cell fusion
Summary
Cancer malignancy is linked to a structural defect in a specific membrane glycoprotein
Area of Science:
- Biochemistry
- Molecular Biology
- Oncology
Background:
- Progressive in vivo cell growth defines malignancy.
- A specific membrane glycoprotein's polysaccharide structure is implicated in malignancy.
- This abnormality is observed across various tumor types.
Purpose of the Study:
- To investigate the link between a specific membrane glycoprotein abnormality and cancer malignancy.
- To confirm the co-segregation of this abnormality with malignancy across cell crosses.
- To validate the abnormality's association with malignancy using lectin-based selection.
Main Methods:
- Analysis of membrane glycoprotein structure in malignant and non-malignant cells.
- Cross-breeding experiments between malignant and non-malignant cells.
- Lectin-based selection of non-malignant variants from tumor cell populations.
Main Results:
- A structural abnormality in a membrane glycoprotein's polysaccharide moiety is consistently found in malignant cells.
- This abnormality co-segregates with malignancy in all tested cell crosses.
- The abnormality remains linked to malignancy even after selecting for non-malignant variants.
Conclusions:
- The identified structural abnormality in the membrane glycoprotein is a reliable marker for malignancy.
- The abnormal glycoprotein is likely a glucose transport protein.
- This finding offers potential for new diagnostic or therapeutic strategies targeting cancer cells.

