In a primary screen, the researchers identified 17 compounds that inhibited
cancer cell adhesion and invasion by at least 75 percent.
Not exact matches
Plakoglobin is a component of two important structures involved in
cell - to -
cell adhesion, and the investigators found that suppressing its expression caused CTC clusters to fall apart, reducing their metastatic potential, and also disrupted
cell - to -
cell contact between breast
cancer cells but not normal breast tissue.
The groundbreaking study identified a protein, known as cadherin - 22, as a potential factor in
cancer metastasis, or spread, and showed that hindering it decreased the
adhesion and invasion rate of breast and brain
cancer cells by up to 90 per cent.
As a doctoral student in the lab of Drs. Margaret Wheelock and Keith Johnson at the University of Toledo, Dr. Islam focused on identifying a link between cadherins (a family of
cell adhesion proteins) and tumorigenesis (start of
cancer cell formation).
The team at Barts
Cancer Institute, part of Queen Mary University of London, have found that a molecule, called focal adhesion kinase (FAK), signals the body to repair itself after chemotherapy or radiotherapy, which kill cancer cells by damagin
Cancer Institute, part of Queen Mary University of London, have found that a molecule, called focal
adhesion kinase (FAK), signals the body to repair itself after chemotherapy or radiotherapy, which kill
cancer cells by damagin
cancer cells by damaging DNA.
In the case of
cancer, ineffective
cell adhesion allows tumour
cells to detach and invade other tissues, thereby spreading
cancer throughout the body.
Once the bacterial
cell signaling protein cagA reaches the host cytosol, it is capable of altering subsequent generations of progenitor
cells, leading to the development of
cancer through changes in mitotic activity, apoptosis, cellular assembly, and signaling.26 Although it should be noted that while the presence of the cagA protein doubles the risk of gastric
cancer, cagA - negative strands also increase the risk of distal gastric
cancer.27 Additional H pylori virulence factors include babA2, which encodes bacterial
adhesion with gastric epithelial
cells, and vacuolating cytotoxin A, which is encoded by the gene vacA.28, 29 H pylori strains carrying some combination of the babA2, cagA, and vacA genes were associated with the highest risk of developing intestinal metaplasia.
This work outlines how a receptor termed LFA - 1 on the surface of T -
cells mediates
adhesion to other
cells such as
cancer cells.
IGFBP5 induces
cell adhesion, increases
cell survival and inhibits
cell migration in MCF - 7 human breast
cancer cells.
The role of tyrosine phosphorylated caveolin - 1 in regulating focal
adhesion dynamics and
cancer cell migration.
Functional expression of CXCR4 (CD184) on small -
cell lung
cancer cells mediates migration, integrin activation, and
adhesion to stromal
cells.
«Many
cancer stem
cells overexpress this surface
adhesion molecule.
MAP3K8 controls
cancer cell proliferation and migration by regulating key players in G1 / S transition and
adhesion dynamics.
Cancer cells attached to endothelial fibronectin deposits via talin1, a major component of focal
adhesions.
Our final review article, from the labs of Maximilian Boesch (Kantonsspital St. Gallen, Switzerland) and Andreas Seeber (Medical University of Innsbruck, Austria), provides an update on the role of epithelial
cell adhesion molecule (EpCAM) in
cancer stem
cells (CSCs) and the epithelial ‐ to ‐ mesenchymal transition (EMT) in colorectal
cancer (CRC).
Based on the glycosylation targets of GalNAc - T6 in the
cancer cell lines, the authors hypothesized that expression of the enzyme disrupts epithelial development in the colon by affecting
cell -
cell adhesion.
Their three - dimensional
cell - culture system, adapted for high - throughput screening, has enabled them to identify small molecules that can inhibit
adhesion and invasion, preventing ovarian
cancers from spreading to nearby tissues.
The company's antibody - based product candidates target a number of potential indications including AL and AA forms of amyloidosis, Parkinson's disease and other related synucleinopathies and novel
cell adhesion targets involved in inflammatory diseases and
cancers.