Bernhard Mlecnik and coleagues examin the impact of tumor - intrinsic, microenvironmental, and immunological factors on
tumor metastasis in colorectal cancer patients.
It has been known for decades that warfarin, the most widely used anticoagulant worldwide, reduces
tumor metastasis in model systems.
Not exact matches
According to Irving Weissman of the Stanford University School of Medicine
in Palo Alto, California: «We showed that even after the
tumor has taken hold, the antibody can either cure the
tumor or slow its growth and prevent
metastasis.»
Aside from the feat of answering the longstanding question of how the lymph system arises, understanding how it forms and develops can provide important insights into disease, from
metastasis to the abnormal accumulation of lymph fluids, particularly
in the wake of surgery to remove cancerous
tumors.
But when their functioning is altered, as the UCL researchers observed
in tumor cells, the mitochondria can promote cell migration, thus leading to the formation of
metastasis.
The discovery of a treatment capable of blocking the mechanism responsible for the formation of
metastasis and the existence of a family of promising compounds, is encouragement for their future assessment
in a clinical study that aims to validate a preventive treatment against
tumor metastasis.
This is one of the first research studies to highlight the importance of the location of the
metastasis as well as the location of the original primary
tumor,
in predicting response to radiation therapy.
Metastasis, the process that allows some cancer cells to break off from their
tumor of origin and take root
in a different tissue, is the most common reason people die from cancer.
Looking to target a key pathway
in order to interfere with the processes that lead to
tumor spread, a research team led by Irwin H. Gelman, Ph.D., of Roswell Park Cancer Institute (RPCI) has identified a new suppressor of cancer
metastasis that may point the way toward development of more effective treatments for prostate cancers and other malignant solid
tumors.
«How melanoma
tumors form: Team identifies drugs that halt skin cancer
metastasis in lab tests.»
MDSCs are immune cells originating from bone marrow stem cells that possess strong immunosuppressive abilities and are known to play a role
in tumor formation and
metastasis.
«This study has provided strong evidence demonstrating that the molecular signature of
metastasis exists prominently
in the primary
tumor,» says Mary Hendrix, a cancer researcher at the University of Iowa
in Iowa City.
In recent years, atypical protein kinase C signaling has been found in the tissue invasion and metastasis of multiple tumor
In recent years, atypical protein kinase C signaling has been found
in the tissue invasion and metastasis of multiple tumor
in the tissue invasion and
metastasis of multiple
tumors.
Runx2 has been linked to bone
metastasis in several solid
tumors, though researchers did not analyze the solid
tumors for expression of bone - related genes.
Last fall, Bergö's group reported that ingestion of extra antioxidants drove the
metastasis of melanoma
in a mouse model, though they didn't have any effect on the primary
tumor.
With these
in vitro test methods, the KU researchers have shown that anti-CD44s antibody can reduce pancreatic cancer cell growth,
metastasis and ability of the
tumors to recur after radiation therapy.
Part of the cytoskeleton, vimentin gives flexibility and structure to the cell, but it is also a marker of epithelial - mesenchymal transition (EMT), which is considered a crucial event for
metastasis in epithelial
tumors.
In addition to potentially improving screening tests, the team believes their approach may someday help doctors control CTC - induced
metastasis, which the researchers say can be far more lethal than the original
tumor.
Their study,
in the journal Oncotarget, is the most extensive analysis to date of gene expression's role
in ccRCC
tumor growth and
metastasis.
Researchers found that genetically disrupting this pathway, or using the FDA - approved Src kinase inhibitor dasatinib, increases PUMA levels and decreases
tumor progression and
metastasis in mice by up to fivefold.
One application is the prognosis of the melanoma: the authors show
in tumor biopsies that the amount of RAB7
in a cutaneous
tumor defines the risk of developing
metastasis.
In an article titled, «Allergen Induced Pulmonary Inflammation Enhances Mammary Tumor Growth and Metastasis: Role of CH13L1,» featured on the cover of the current issue of the Journal of Leukocyte Biology, this new research suggests inflammation raises the level of a known biomarker of cancer, called «chitinase -3-like-1» or «CHI3L1,» in the inflamed tissue, which leads to increased metastasis and faster cancer growth in that tissu
In an article titled, «Allergen Induced Pulmonary Inflammation Enhances Mammary
Tumor Growth and
Metastasis: Role of CH13L1,» featured on the cover of the current issue of the Journal of Leukocyte Biology, this new research suggests inflammation raises the level of a known biomarker of cancer, called «chitinase -3-like-1» or «CHI3L1,» in the inflamed tissue, which leads to increased metastasis and faster cancer growth in th
Metastasis: Role of CH13L1,» featured on the cover of the current issue of the Journal of Leukocyte Biology, this new research suggests inflammation raises the level of a known biomarker of cancer, called «chitinase -3-like-1» or «CHI3L1,»
in the inflamed tissue, which leads to increased metastasis and faster cancer growth in that tissu
in the inflamed tissue, which leads to increased
metastasis and faster cancer growth in th
metastasis and faster cancer growth
in that tissu
in that tissue.
This blood vessel normalization results
in an increased barrier function on the one hand — thereby blocking cancer cell dissemination and
metastasis - and
in enhanced
tumor perfusion on the other hand, which increases the response of the
tumor to chemotherapy.
Cheng and colleagues did experiments using human cells and identified hnRNPM's role
in controlling the processes linked to
tumor metastasis.
According to Semenza, «Chemotherapy may kill more than 99 percent of the cancer cells
in a
tumor but fail to kill a small population of cancer stem cells that are responsible for subsequent cancer relapse and
metastasis.»
Loss of either GSTO1 or RYR1, the researchers report, decreased the number of cancer stem cells
in the primary
tumor, blocked
metastasis of cancer cells from the primary
tumor to the lungs, decreased the duration of chemotherapy required to induce remission and increased the duration of time after chemotherapy was stopped that the mice remained
tumor - free.
Where these three cells come
in contact is where
tumor cells can enter blood vessels — a site called a
tumor microenvironment of
metastasis, or TMEM.
Treatment with an investigational CAR T - cell therapy induced complete remission of a brain
metastasis of the difficult - to - treat
tumor diffuse large - B - cell lymphoma (DLBCL), which had become resistant to chemotherapy — the first report of a response to CAR T - cells
in a central nervous system lymphoma.
Investigators found that NPTX2 was expressed
in all stages of kidney cancer, especially
metastasis, which suggests it plays an important role
in tumor development and progression.
«Now we're investigating how the protein works
in order to be able to develop a drug that could prevent
tumor metastasis.»
«However, IL6 - secreting
tumors could be laying the groundwork for
metastasis much earlier than surgery occurs
in a patient,» he said.
The work also reinforces the importance of finding
tumor cell clusters
in the blood as a mechanism of detecting cancer
metastasis earlier.
So making cells
in the primary
tumor softer might be a way to prevent
metastasis,» he said.
When the protein is present, these cells that start out round and stuck together
in a pattern resembling cobblestones become irregularly shaped and tend to detach from the
tumor site
in an uncoordinated way — hallmarks of
metastasis.
The study also indicated that genomic diversity may also have useful clinical applications for predicting
tumor invasion,
metastasis and poor survival
in patients.
«
In the future, our models should provide robust tools to screen for therapies that impact
tumor dormancy and
metastasis, and should also provide a platform to solve other biological mysteries that underlie dormancy.»
By viewing this fusion as another disease imposed onto
tumor cells, scientists could devise new therapies against
metastasis, the researchers say
in the May Nature Reviews Cancer.
«STAT3 is the primary marker that is used today to ascertain malignancy,
tumor aggression and
metastasis in ovarian cancer.»
«The result was an extensive inhibition of
tumor growth and prevention of
metastasis to the lung
in HER2 - positive animal models of breast cancer,» notes Navasona Krishnan, Ph.D., a postdoctoral investigator
in the Tonks lab who performed many of the experiments and is lead author on the paper reporting the results.
By identifying the cause of this
metastasis — which often happens quickly
in lung cancer and results
in a bleak survival rate — Salk scientists are able to explain why some
tumors are more prone to spreading than others.
So that's pretty good because
metastasis is what kills you
in cancer, not the primary
tumor.
She is investigating the role of glycosylated molecules
in tumor progression and
metastasis, tissue - and species - specific expression of lectin receptors that play a role
in regulating host innate immune responses and inflammation, and the immunological mechanisms underlying chronic inflammation and cancer development.
Tumor metastasis is the primary cause of mortality
in cancer patients and remains the major challenge for cancer therapy.
Metastasis (the spread of cancer from its primary site to other places
in the body) to the ovaries can result
in Krukenberg
tumors.
«We found that many more mice developed
tumors when given the cells that we had engineered to have these stem cell characteristics, and they had a much higher incidence of
metastasis in the lungs,» Kilian said.
In a four - year study conducted on the mouse model in advanced breast cancer metastasis in the eye's anterior chamber, Petty and colleagues found that the new nanoparticle not only killed tumor cells in the eye, but also extended the survival of experimental mice bearing 4T1 tumors, a cell line that is extremely difficult to kil
In a four - year study conducted on the mouse model
in advanced breast cancer metastasis in the eye's anterior chamber, Petty and colleagues found that the new nanoparticle not only killed tumor cells in the eye, but also extended the survival of experimental mice bearing 4T1 tumors, a cell line that is extremely difficult to kil
in advanced breast cancer
metastasis in the eye's anterior chamber, Petty and colleagues found that the new nanoparticle not only killed tumor cells in the eye, but also extended the survival of experimental mice bearing 4T1 tumors, a cell line that is extremely difficult to kil
in the eye's anterior chamber, Petty and colleagues found that the new nanoparticle not only killed
tumor cells
in the eye, but also extended the survival of experimental mice bearing 4T1 tumors, a cell line that is extremely difficult to kil
in the eye, but also extended the survival of experimental mice bearing 4T1
tumors, a cell line that is extremely difficult to kill.
Metastasis is the process
in which cells from a primary
tumor break - off, enter the blood stream and create new
tumors elsewhere
in the body.
This allows cancer cells to break off from
tumors, spread throughout the body (
in blood or other fluid) and form new
tumors at distant sites — a process called
metastasis.
It is not easy to determine whether
metastasis began early or late
in the development of the primary
tumor or whether individual metastatic sites were seeded directly from the original
tumor or from an intermediate site.
The authors note that there are two different models of
metastasis — one
in which an advanced primary
tumor disseminates metastatic cells late
in its development, which would predict little genetic difference between primary and metastatic cells, and another
in which
metastasis occurs early
in tumor development, which would predict significant genetic differences
in metastatic cells that have evolved separately from those
in the primary
tumor.