Correlation between invasiveness of colorectal tumor cells and adhesive potential under flow

Autor: Benoliel, A. M., Pirro, N., Marin, V., Consentino, B., Pierre Bongrand, Vitte, J., Bongrand, P., Sielezneff, I., Sastre, B.
Přispěvatelé: Adhésion et Inflammation (LAI), Assistance Publique - Hôpitaux de Marseille (APHM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), Service de Chirurgie Digestive (AP-HM), Université de la Méditerranée - Aix-Marseille 2, Bongrand, Pierre, Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2003
Předmět:
MESH: Antigens
CD29

MESH: E-Selectin
Vascular Cell Adhesion Molecule-1
[SDV.BBM.BP] Life Sciences [q-bio]/Biochemistry
Molecular Biology/Biophysics

MESH: Flow Cytometry
[SDV.CAN]Life Sciences [q-bio]/Cancer
MESH: Cadherins
MESH: Cell Adhesion
[SDV.CAN] Life Sciences [q-bio]/Cancer
Antigens
CD

Cell Adhesion
Humans
Neoplasm Invasiveness
MESH: Antigens
CD

MESH: Antigens
CD18

MESH: Colonic Neoplasms
MESH: Humans
MESH: Stress
Mechanical

Rectal Neoplasms
Integrin beta1
MESH: Vascular Cell Adhesion Molecule-1
MESH: Biological Markers
MESH: Rectal Neoplasms
MESH: Neoplasm Invasiveness
Cadherins
Flow Cytometry
[SDV.BBM.BP]Life Sciences [q-bio]/Biochemistry
Molecular Biology/Biophysics

CD18 Antigens
Colonic Neoplasms
MESH: Cell Adhesion Molecules
Stress
Mechanical

E-Selectin
Cell Adhesion Molecules
Biomarkers
Zdroj: Anticancer Research
Anticancer Research, International Institute of Anticancer Research, 2003, 23 (6C), pp.4891-6
Anticancer Research, 2003, 23 (6C), pp.4891-6
ResearcherID
ISSN: 0250-7005
Popis: International audience; BACKGROUND: Tumor cell adhesiveness is involved in metastatic dissemination, and adhesive behavior may be different under static and dynamic conditions. MATERIALS AND METHODS: Patients undergoing primary colorectal cancer excision were tested for: i) serum concentration of sE-selectin, sICAM-1 and sVCAM-1, ii) expression of CD18, CD29d and E-cadherin on tumor cells and iii) efficiency of tumor cell adhesion to ECV304 monolayers under flow and resistance to detachment by shear. RESULTS: Twenty out of 31 patients were free of detectable relapse 12 months later. Relapsing and non-relapsing patients had similar levels of soluble adhesion molecules. E-cadherin was detected on tumor cells from three non-relapsing patients, but no relapsing one. Unexpectedly, significant CD18 labeling was found on two relapsing patients and one non-relapsing patient. Cells from relapsing patients displayed significantly increased (p < 0.05 two-sided, p < 0.025 one-sided) capacity to adhere to test monolayers under flow. CONCLUSION: Cancer invasion is related to tumor cell adhesiveness, and the flow chamber provides a practical way of measuring adhesive parameters with a potential value for relapse prediction.
Databáze: OpenAIRE