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katherine-medina

The Efficacy of Dandelion Root Extract in Inducing Apoptosis in Drug-Resistant Human Me... - 0 views

www.ncbi.nlm.nih.gov/...PMC3018636

Dandelions Cancer-fighting botany HSR-2023 potential research idea Melanoma

shared by katherine-medina on 07 Jun 23 - No Cached
Sean Nash liked it
  • 2. Materials and Methods
  • 2. Materials and Methods
    • katherine-medina
      katherine-medina on 07 Jun 23
       
      If I plan on doing some sort of experiment with Dandelion root, I will likely need to come back and look at how this study did it.
  • After a long exposure of 96 hours, NHFs did not exhibit any reduction in cell viability
    • katherine-medina
      katherine-medina on 07 Jun 23
       
      Wow, so even after 3 days the Dandelion Root did nothing to the NHF aka. normal human cells.
  • ...15 more annotations...
  • With DRE having proven its efficacy in successfully killing this aggressive, chemoresistant form of skin cancer, DRE toxicity on normal cells had to be evaluated
    • katherine-medina
      katherine-medina on 07 Jun 23
       
      Always remember to hav e a control.
  • DRE was found to reduce cell viability in a dose-dependent fashion, over time, in A375 melanoma cells as was measured by WST-1 assay. Based on metabolic activity of A375s, it was confirmed that treatment at 2.5 mg/mL DRE resulted in ~50% reduction in cell viability against control within 24 hours (Figure 1(a))
  • Higher doses were then used and a response was observed at a concentration of 10 mg/mL (
    • katherine-medina
      katherine-medina on 07 Jun 23
       
      For different types of melanoma a different amount of DRE is needed.
  • Typical apoptotic morphology was observed in G361 cells treated with DRE starting at 5 mg/mL concentrations for 72 hours
  • . However, there has been little scientific advancement made in this field with regard to the effect of dandelion root extract on cancer, and even more so on chemoresistant, human malignant melanoma skin cancer.
    • katherine-medina
      katherine-medina on 07 Jun 23
       
      I do so love it when the author identifies the fact that there is so few research papers about DRE.
  • ) is more than a worthy chemopreventative, it is fast-acting, nontoxic, and therefore specific in its targeting of human melanoma cancer cells, making it a valuable chemotherapeutic. We have investigated the induction of apoptosis in human malignant melanoma cells and observed its long-term effects in human melanoma cancer.
    • katherine-medina
      katherine-medina on 07 Jun 23
       
      alrighty then.
  • We are yet to determine the effect of each of the individual components (such as the family of triterpene alcohols and phenolic acids—found in the roots—and cinnamic acids, flavinoids and coumarins—that are found in the leaves
    • katherine-medina
      katherine-medina on 07 Jun 23
       
      Maybe I could look into the specific component that kills the cancer, so that in future years after I had figured this out I could put it into practice.
  • Given that DRE has traditionally been used naturopathically for a variety of ailments, we assume that it would be relatively nontoxic to healthy cells. Our results show that the Normal Human Fibroblasts (NHFs) (which were treated at a low population doubling where NHFs have the best proliferation rate) and Peripheral Blood Mononuclear Cells remained unaffected and healthy after a 96-hour and 48- hour exposure to DRE, respectively (Figures 2(a)–2(d)).
  • Lupeol,
    • katherine-medina
      katherine-medina on 07 Jun 23
       
      What is Lupeol. (I should probably look into that.)
  • taraxasterol
  • More importantly, an increase in ROS production indicates prooxidant behaviour of DRE on cancer cell mitochondria, which is contrary to the antioxidant convictions of traditional medicine and previous studies on Taraxacum extracts citing reductions in NO, ROS, RNS, and COX-2 [10, 11] in mouse macrophages.
    • katherine-medina
      katherine-medina on 07 Jun 23
       
      That is very important and interesting.
  • There are two main points that must be stated here: firstly, that noncancerous cells are unaffected by DRE treatment, and secondly, melanoma cells retain the signals to commit suicide long after DRE has been removed from the system
    • katherine-medina
      katherine-medina on 07 Jun 23
       
      Good to restate.
  • Metformin acts as a metabolism interfering compound that debilitates cancer cells, and the case of G361-resistant melanoma cells, combining DRE with metformin reduces cell viability at even lower doses (Figures 9(a) and 9(b)).
  • By 48 hours, human melanoma A375 cells uncharacteristically showed susceptibility to apoptosis induction by DRE
  • We believe that this nontoxic extract can undergo precipitous translation from bench top to bedside, with dandelion products that are already commercially available in the form of tea and supplements.
  • katherine-medina on 07 Jun 23
     
    Essentially it is an article that figured out that DRE can induce apoptosis in melanoma cells, and it also proved that DRE is non-toxic to normal human cells.
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