If tumor cells are not present in the sentinel node, the primary tumor most likely has not spread to lymph nodes or other organs.
If tumor cells are present within the node, the primary tumor has spread and additional lymph nodes may need to be removed and medical treatments tailored accordingly.
Aware that cancers rewire their metabolism in ways that could change the epigenome and that distant metastases in pancreatic cancer naturally spread to organs fed by a sugar - rich blood supply, the researchers wondered
if the tumor cells had altered the way they use the basic form of sugar, glucose.
Not exact matches
So even
if a
tumor is surgically removed, it is difficult to extract every cancerous
cell; any left behind will result in the growth of a new
tumor.
«For pro-life folk, imagine a country where it was illegal to remove a
tumor, even
if the
tumor might kill the host, because the
tumor is its own collection of living
cells.
But that gives scientists a secret weapon —
if they can harness stem
cells» natural ability to «home» toward
tumor cells, the stem
cells could be manipulated to deliver cancer - killing drugs precisely where they are needed.
If we are able to keep the
tumor cells contained and let them fight it out, we would expect to see more competitively fit
cells that are growing very slowly.»
If the
tumor that Jobs had removed in 2004 had begun to break down prior to the surgery, White says, the
tumor's dead
cells could have released protease and lipase enzymes that may have damaged beta
cells in the pancreas, which produce insulin.
Along with the study's co-first authors, Drs. Aayoung Hong and Gatien Moriceau, Lo hypothesized that
if they could identify the key
tumor cell processes triggered by withdrawal of MAPK inhibitors, then scientists can exploit these process with existing or investigational drugs to trigger the maximal levels of
tumor cell death immediately following cessation of the initial therapy.
If we can boost the immune system and allow microglia to do their job and control brain
tumor stem
cells, it would be like removing the seed from the soil — stopping the
tumor growth before it starts to get out of control.»
You have T
cells for the rest of your life, so
if the
tumor reoccurs those T
cells can mobilize themselves again against the
tumor.
«
If we can identify the point at which
tumor cells acquire the characteristics of stem
cells, it will be possible to look for ways to interrupt the process and avoid progression of the disease.»
«We know that
if you take these
tumor cells out of a patient and put them in a petri dish, they can be killed by chemotherapy,» Beatty said.
According to Dr. Cripe, the study suggests that some patients could respond to therapy even
if their
tumors aren't very infectable by the virus, provided their immune systems were stimulated by the viral therapy to attack the
tumor cells.
The arithmetic is complex, but the consensus is that, to pose a health threat, cancers have to replicate at least 200 to 300 times, even though a clinically relevant
tumor contains «only» a million million
cells, which could be achieved by «only» 40 or so divisions
if the originating
cell had all the necessary mutations from the outset.
If they can be used in living tissue, they might eventually track
cells in developing embryos, the immune system, or cancerous
tumors.
If a given drug cocktail kills 90 percent of the cancer
cells but doesn't affect the remaining 10 percent, the resistant
tumor cells can take over and cause the
tumor to grow back.
They found that
if autophagy — the intracellular recycling process — is blocked in
tumor cells, they produce cytokines that attract NK
cells.
If metastatic cancers are most often made up of
cells with different genetic drivers, perhaps researchers should be targeting the primary
tumor with multiple drugs to contain the cancer.
The modified T
cells are then reinfused back into a patient and,
if all goes well, attack the person's NY - ESO - 1 — displaying
tumors.
If the stem
cells lose Numb, however, p53 levels plunge and the
cells proliferate uncontrollably, leading to the emergence of cancer stem
cells that drive the growth of breast
tumors.
In human
cells as well,
if Nbs1 and ATM function in the same way to ensure repair of DNA damage,
tumor formation may be prevented.
To see
if PGD and the pentose phosphate pathway were tied to the epigenetic changes the researchers had detected in distant metastases, they treated
tumor cells from different sites in a single patient with the drug 6 - aminonicotinamide (6AN), which is known to inhibit PGD but is not used in humans because of its severe side effects.
«We have shown that our molecule works on cancer
cells in the lab, but the next step is to see
if it works on real
tumors in animals.
If the signaling error occurs before the
cells have differentiated to become either bone or hair or skin, the result can be a teratoma, a
tumor that contains a jumble of
cell types.
«The
cells that escape detection are the ones that,
if not removed, are the most likely to result in treatment failing and a
tumor recurring.
In experiments involving mice injected with human GBM
cells, the scientists also demonstrated that
if either PTEN or DAXX were eliminated, then
tumor growth occurred.
The light - sensitive
cells and nanoparticles, called opto - CRAC, were then delivered with the
tumor antigen surrogate ovalbumin to mice with melanoma
tumors in their lymph nodes to see
if an immune response could be activated to target cancer
cells.
If the targeted RNA encodes a
tumor suppressor protein, as scientists have found for some, the ultimate effect of the microRNA could be to promote
cell — and
tumor — growth.
Encouraged by these results, the scientists wondered
if Listeria could be used to deliver cancer - fighting therapies straight to
tumor cells, including metastatic ones.
They work particularly well
if the cancer
cells they attack already have defects in the corresponding DNA repair pathways, as it frequently occurs in breast cancer and other
tumors.
In the new study, the researchers cultured mouse skin - cancer colonies on various 2 - D and 3 - D environments of different shapes and patterns to see
if the
tumor shape contributes to activation of cancer stem
cells, and to see where in the
tumor the stem
cells appeared.
«
If the CD117
cell population does lead to
tumor initiation or cancer reoccurrence, this
cell marker could become a therapeutic target,» she says.
Researchers believe that
if the body contains enough of the protein, the immune system will recognize it as a potential danger and send out armies of disease - killing
cells to seek and destroy
tumors harboring it.
And
if fetal
cells protect women from breast cancer, they might also safeguard against other
tumors.
This is essential
if one wants to claim that the
cells, and thereby the research results, are true representatives of the original
tumor.
«These slow - growing
cells are apparently kept in check by the rest of the
tumor, somehow — indeed,
if you remove them from a
tumor, they grow like crazy.»
«In extreme cases,
if the dose is too high radiation can modify the cellular structure and generate alteration in the
cells of organs found near the
tumor, this causes them to lose their functions,» said Massillon, who was honored for her research with the IUPAP Young Scientist Prize 2015 awarded by the International Union of Pure and Applied Physics.
If a
cell fails to produce the ultraconservated RNA, microRNA gets altered and hundreds of genes that should maintain cellular balance does and thus contributes to the formation of human
tumors,» concludes Manel Esteller.
Numerous studies have already shown that cancer spreads particularly aggressively
if there is an unfavorable balance between suppressing and active immune
cells in the
tumor microenvironment.
Overall, including all genomic variations present in most
if not all
tumor cells (clonal) as well as those present only in subsets of the cancer
cells (subclonal) from
tumor tissue, the researchers detected a total of 864 genetic changes in tissue samples across the three
tumor types, and 627 (73 %) of those were also found in the blood.
If it is, we know that the Y - 90 DOTATOC radiotherapy will also reach the
tumor and be able to kill
tumor cells.»
The identification of patients with high - risk breast cancer is key to knowing whether a patient will require only the removal of the
tumor by surgery or whether
if she will need additional chemotherapy to make sure the removal of breast cancer
cells.
The problem, said Lin, is that
if a
tumor has been growing for years there are no longer any T -
cells inside it to activate, so the therapy fails.
«
If we can confirm that substantial signal levels originate from glucose in the
cell interior, this would be important additional information for
tumor imaging and functional MRI.
What's more, the drug also increased the immune system's «memory»
cells so that they could attack the
tumor if it ever reared its head again.
If you're hoping the loudmouth on the
cell phone next to you will get a brain
tumor, you're likely to be disappointed.
We decided to look at the exosomes of stromal
cells, a type of
cell that is commonly found in the
tumor microenvironment, and see
if stromal exosomes were influencing the energy consumption of cancer
cells.»
«
If you were to compromise the altered physiology of
tumors with something like RHT, the cancer
cells are going to be less able to tolerate other therapeutic insults, and that probably would give you more effective therapies.
Next they treated the experimental
tumor cells with MIR506 to determine
if it would behave in the same way it had with ovarian and other cancers.