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In a recent five-year study of nearly 30,000 rural Chinese people, researchers from the NCI found that daily doses of these three nutrients reduced cancer deaths by 13%.

In a study in Cancer Letters (Evangelou et al. 1997), animals with malignant tumors given high doses of vitamins C and E and selenium manifested a significant prolongation of the mean survival time. Complete remission of tumors developed in 16.8% of the animals

cities and states with high selenium content in the soil also had significantly lower rates of cancer, especially of the digestive and urinary systems.

In one study of hundreds of men, a daily intake of 200 micrograms of selenium cut the incidence of prostate cancer by 60 percent.

The statistics for breast cancer are particularly striking. "The higher the selenium, the lower the breast cancer

In Yugoslavia, scientists studied 33 patients with breast cancer. These women had selenium levels in their bloodstream only half those of healthy volunteers.

The overall reduction in cancer incidence was 37% in the selenium-supplemented group; a 50% reduction in cancer mortality was observed over a 10-year period

The following are the site-specific reductions in cancer incidence observed in the study: colon-rectal cancers (58%), lung cancer (46%), and prostate cancer (63%)

A selenium deficiency appears to increase the risk of prostate cancer fourfold to fivefold

It was determined that, as the male population ages, selenium levels decrease, paralleling an increase in prostate cancer

NK cells are large granular lymphocytes that comprise approximately 10 % of circulating lymphocytes

all human NK cells express the CD56 antigen

treatment with various concentrations of IL‐2 in vivo may induce distinct functions within the NK cell compartment and, therefore, may have profound effects on NK cell‐mediated cytotoxicity

CD56bright

CD56dim

We show here that ADCC conducted by NK cells in vitro is enhanced by IL‐2 activation and is critically dependent on interactions between FcγRIII on NK cells and Herceptin‐coated tumor targets

administration of low‐dose IL‐2 to patients results in the marked expansion of a CD56+ population of immune effectors with the ability to lyse antibody‐coated cancer targets

NK cells represented only 7 % of lymphocytes prior to therapy but comprised over 50 % of the population after 10 weeks of low‐dose IL‐2

These data suggest that the enhanced ADCC seen following the expansion of NK cells with low‐dose IL‐2 is likely due to an increase in the overall number of NK cells

co‐administration of IL‐2 with rhu4D5 mAb will enhance activation of NK cell effector functions

Stimulation of NK cells with IL‐2 resulted in a significant increase in the lysis of rhu4D5‐coated targets

We have shown that costimulation with IL‐2 plus rhu4D5 results in significant production of IFN‐γ by NK cells with concomitant up‐regulation of cell‐surface activation and adhesion molecules

It has been previously demonstrated that continuous low‐dose IL‐2 can expand a CD56+ lymphocyte population, and we have now shown that this cell population is a potent mediator of ADCC against rhu4D5 mAb‐coated Her2 / neu+ targets

These results suggest that administration of low‐dose IL‐2 can be used to expand NK cell numbers, while higher doses may be used to enhance their cytolytic capacity in the setting of mAb therapy

we have demonstrated that NK cell lysis of Her2 / neu+ breast cancer cell lines in the presence of rhu4D5 mAb is markedly enhanced following stimulation with IL‐2

we have presented evidence that administration of low‐dose IL‐2 in vivo results in the expansion of a potent NK cell effector population

Our experiments suggest that NK cells costimulated with IL‐2 and immobilized IgG can secrete potent immunomodulatory cytokines which may serve to potentiate the anti‐tumor immune response.

no treatment-related deaths

the most common adverse events were anaemia (26 [70%]), fatigue (25 [68%]), and rash

hypothyroidism

hypothyroidism

nivolumab-related autoimmune hypothyroidism, which resolved after a short course of corticosteroids

No grade 3 or 4 adverse events occurred

Nivolumab resulted in objective responses in 24% of patients with metastatic SCCA

Historically, doublet chemotherapy with cisplatin and fluorouracil has been the most common treatment for patients with metastatic SCCA

our results suggest that immune checkpoint blockade agents might extend overall survival beyond currently available therapies, especially if provided early in the disease treatment course

the dose of nivolumab we used differs from the 2016 recommendation of a fixed 240 mg every 2 weeks

25% of patients develop distant metastases

most patients with localised SCCA are cured by chemoradiation

More than 90% of cases of SCCA are linked to prior infection with human papillomavirus (HPV)

Within tumour cells, HPV oncoproteins are immunogenic and can trigger an anti-tumour host immune response by recruitment of tumour-infiltrating lymphocytes

Tumour cells express PD-L1 and, on binding its inhibitory receptor PD-1 on the surface of T cells, downregulate T-cell activation and thwart the local anti-tumour immune response

Nivolumab is a humanised monoclonal antibody against PD-1 that disrupts this interaction, enabling T-cell cytotoxicity. It has activity as a monotherapy in advanced solid cancers, such as head and neck cancer, melanoma, non-small-cell lung cancer, and renal cell carcinoma

This broad effect could be a result of niclosamide's pleiotropic activity, similarly affecting signaling pathways that are known to be overly active in human malignant cells (i.e., mTOR, NOTCH, WNT/CTNNB1; refs. 44–46)

It is a salicylanilide that was introduced as a molluscide in 1959

Studies in animals suggested no mutagenic, oncogenic, or embryotoxic activity and no cumulative effects

its rate of absorption from the intestinal tract was estimated at only 33%

the potential mechanism of synergy between temozolomide and niclosamide as a “natural inducer” of NFKBIA

Ovarian cancer stem cells play an important role in chemoresistance and cancer recurrence

Furthermore, recent studies indicate that niclosamide exhibits anticancer effects against various human cancer cells by acting on multiple cell signaling pathways and inducing mitochondrial uncoupling [16–21]

has low systemic bioavailability (~10%) when administered orally, which is beneficial for treating local parasitic infections of the intestines while minimizing systemic exposure

The nano-NI demonstrated significantly higher inhibitory effects on sphere formation than the original niclosamide did

the nano-NI formulation decreased the metabolic activity of ovarian cancer cells and caused a metabolic shift from oxidative phosphorylation to glycolysis

This toxicity evaluation showed that oral nano-NI had no toxic effect on either group of mice in terms of weight, plasma albumin levels, and blood cell counts, and revealed no adverse effects on vital organ function in the rodents, which suggests that nano-NI is safe for animals

niclosamide inhibits tumor cell growth by interrupting multiple pathways (Wnt, Notch, STAT3, NF-κB, and mTORc1) and the generation of reactive oxygen species in several cancer cells

The current standard therapy for ovarian cancer includes taxanes and platinum-based chemotherapy after cytoreductive surgery. Among treated patients, nearly 70 to 80% will experience disease recurrence

The safety of HBOT was also evaluated and it was pointed out that, if given at proper paradigms, like 1.5 ATA for 60 minutes, HBOT will not cause oxygen toxicity

Rockswold et al., on the other hand, found that HBOT might be potentially beneficial for severe TBI patients

McDonagh et al., concluded that there was insufficient evidence to establish the effectiveness of HBOT in the treatment of TBI

The first multicenter, randomized, double-blind, controlled trial in 2009 found that 40-hour HBOT of 24% oxygen at 1.3 ATM produced significant improvement in children's overall functioning, receptive language, social interaction, eye contact, and sensory/cognitive awareness compared to those received slightly pressurized room air

Another study in 2010 on 16 autism patients, adopting a similar treatment paradigm, showed no effect on a wide array of behavioral evaluations

To date, there is little evidence that HBOT causes malignant growth or metastasis. A history of malignancy should therefore not be considered as a contraindication for HBOT

HBOT enhances the production of reactive oxygen species (ROS) and causes oxidative stress in body tissues

Excessive accumulation of oxidative stress may contribute to neurodegenerative processes and cell death in the brain, as seen in diseases like Alzheimer's disease (AD) and Parkinson's disease (PD)

Hormesis

process that results in a functional improvement of cellular stress resistance, survival, and longevity in response to sub-lethal levels of stress