Neuroblastoma And Microrna-34a

Great Essays
Neuroblastoma and microRNA- 34a is commonly mentioned together in many articles and studies around the world. With the advance in medicine and new discoveries, there has been found a dependence relation of neuroblastoma with these specific type of microRNA since it has been discovered how it could eliminate cancer eternally. MicroRNA-34a has not only revolutionized scientists but the world in general because of its ability to destroy neuroblastoma but also because is a new natural genetic regulator of a tumor suppressor. Its level of dominance allows it to control different processes like apoptosis, metastasis, and differentiation in the cell cycle. MicroRNAs have taken control over diverse organisms, not only humans but also plants …show more content…
The human genome has thousands of different types that are usually found in human’s genes and mammals. One of the most important is microRNA-34a. It acts as a regulator of the suppression of tumors in the human body. When cancer is present, transcription factors are not able to bind with the double helix strand because the exact sequence required is not present due to a mutation in the DNA strand. MicroRNA 34a plays the role of the transcription factor that was supposed to stick. Combined with proteins and receptors, microRNA 34a is capable of preventing the division of cell (Misso, …show more content…
When the DNA is damaged, it automatically activates the p53 gene. p53 or usually known as a tumor protein, attaches to miR-34a promoter in order to normalize the expression of microRNAs. p53 eliminates the opportunity for a tumor to occur in correlation with transcriptional targets and having miR-34a to the side in order to avoid any inappropriate cell propagation. Likewise, any damage in the DNA signaling could affect the evolutionary biogenetics process from the p53 gene activation. MicroRNA-34a together with p53, activate SIRT-1, a protein that catalyzes NAD- dependent deacetylation (Rahman, 2011). When SIRT-1 is activated, facilitates the survival of cells through long stages of stress. MicroRNA-34a attaches to SIRT-1 to increment p53 action and move acetyl to different molecules. As this mechanism occurs, it allows to increase and intensify p53 stabilization which would have allowed the cell to be protected with the positive feedback loop. This provides the cell a better living environment where is not being affected by any damages in the DNA or cellular pressure. Bioinformatics estimates propose that a grand amount mRNAs possess equivalents to miR-34a sequence. New studies have discovered how microRNA-34a is crucial in neuroblastoma tumorigenesis, which permits researchers and doctors to observe the power and importance of miR-34a in the human body

Related Documents

  • Decent Essays

    Angiogenesis is complex, dynamic process involving the migration, growth, and differentiation of endothelial cells, and orchestrated by a balance of pro and anti-angiogenic signaling pathways. It is an early and crucial step alleviating the tumour progression and metastasis. Important stimolator of angiogenesis are Vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF2), angiopoietins (ANGPT1 and ANGPT2), Notch ligands [jagged 1 (JAG1) and Delta like ligand 4 (DLL4) and transforming growth factor-β (TGF-β). miRs are important for vascular development, physiology, and disease however, only a few specific miR-NAs targeting angiogenesis have been identified, till date. Downregulation of the miRNA-processing enzymes Dicer and…

    • 133 Words
    • 1 Pages
    Decent Essays
  • Improved Essays

    Most cancer results from faulty DNA repair mechanisms. 40. Cells become cancerous from point mutations (CpG transition in p53), double-stranded breaks, major chromosome rearrangements, chromosome loss/gain, loss of checkpoints, activation of oncogenes, and turning off tumor suppressors via hypermethylations. 41. Mutations and chromosomal abnormalities will affect the regulation of proteins or the structure of the proteins.…

    • 1697 Words
    • 7 Pages
    Improved Essays
  • Improved Essays

    The simple but revolutionary organism Drosophila melanogaster has intricate properties that are studied to find its relations with human genes. Not only is D. melanogaster a model organism for its rapid growth, inexpensive culturing, and easy modifications, the Drosophila can provide more in-depth scientific analysis that can solve human diseases. The model organism D. melanogaster is studied to find ground-breaking research in neurology, sleep, cancer, and drug discovery. The multivariable effects in cancer can be studied by observing D. melanogaster because of its tumorigenesis caused by genes and its surrounding environment. The development of tumors in D. melanogaster is similar to the pathway of a tumor in a mammalian cell as it undergoes…

    • 1018 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    P 53 also known as “the guardian of the genome” is a tumor suppressor gene that works regulating the cell cycle and apoptosis. It is a very important gene since the lack of its action can allow the cells to divide an abnormal number of times and if action is not taken by the cell’s checkpoints, this could lead to cancer. The evolution of tumors associated with mutations in the p53 gremlin is not well understood and numerous researches have been completed trying to identify all of its characteristics. As all inherited gene mutations, p53 mutations are present in all somatic cells, but the effect of these mutations can have malignant effect on the cells.…

    • 212 Words
    • 1 Pages
    Improved Essays
  • Improved Essays

    Annotated Bibliography

    • 581 Words
    • 3 Pages

    Blood 123(18), 2816-25(2014). PMID 24574459 When observing splicing of RNA in cells of AML patients, scientists observed abnormal spliced genes of NOTCH2 and FLT3. These genes hold the blueprint for myeloid cell surface proteins. This abnormality is present in over 70% of AML patients, suggesting that it may be responsible for the production of proteins with malignant functions. May also correlate to the progression of AML.…

    • 581 Words
    • 3 Pages
    Improved Essays
  • Decent Essays

    Grade IV astrocytomas are two types i.e Primary and secondary tumors , as we know that primary tumors are very aggressive and the most common form of astrocytoma grade IV [19] and the secondary tumors are those which originate as a lower-grade tumor and evolve into a grade IV tumor. It is distinguished histopathologically from diffuse lower-grade astrocytomas by the presence of necrosis or micro vascular proli-feration[20].Among several tumor suppressor genes, p53 reveal to play a key role in the pathogenesis of many prevalent malignancies [21] including brain cancer. p53 has been displayed to exert tumor suppressor activity by impelling apoptosis , initiating the cell cycle [22], stimulating cell differentiation [23], and being involved in DNA repair pathways [24]. Mutations in the p53 gene are identified in about 28% of de novo GBM and 65% of secondary [25], thus indicating that p53 abnormalities are common in the progression from a low grade lesion to a high grade lesion…

    • 334 Words
    • 2 Pages
    Decent Essays
  • Improved Essays

    Uranium Affects TP53

    • 678 Words
    • 3 Pages

    The gene has a very important location in the nucleus of our cells, where it binds directly to DNA. When DNA is…

    • 678 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Non-Coding In Malat1

    • 474 Words
    • 2 Pages

    The objective of the first problem summary assignment was to compose an essay illustrating the impact of non-coding on gene expression, utilize primary articles to discuss the role of specific non-coding RNA molecules in the transcriptome, and examine the implications of current study on future research. In order to accomplish this, I analyzed and summarized the primary research article by Chen et al., which discussed the role of Malat1 in cellular proliferation and differentiation. Once I developed a general understanding of the purpose, methods, and results of the article I began looking for other papers to supplement the primary source and provide me with a better understanding of the context of the paper. Once I understood the physiological process of…

    • 474 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    The Integumentary System is the largest body system of humans. Being the largest there can be a larger number of possible issues, than other body systems. Skin cancer is a growing issue in this country. Cutaneous Squamous Cell Carcinoma is one of the most common forms of skin cancer. Our very own sun can cause this cancer, also causing it to advance from the Ultraviolet Rays.…

    • 513 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Metastatic Brain Tumors

    • 523 Words
    • 3 Pages

    Thus, we are in need of such information and models for development of new, efficient therapies. The essential role of the tumor microenvironment in cancer progression has been well documented for many…

    • 523 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    The AKT1 gene belongs to a category of genes called “oncogenes”, which can potentially cause cells to become cancerous or exhibit cancer-like qualities when mutated, depending on the type of mutation present. The exact cytogenetic location of this mutation, an activating mutation officially called “c. 49G>A, p.Glu17Lys”, is notated as 14q32.32. As stated previously, cells containing this AKT1 gene mutation are unable to regulate their own division and growth, thus leading to increased cell proliferation as well as abnormal development. Additionally, this mutation prevents cells from dying off through a process called apoptosis, even if they begin to exhibit properties that would normally prompt them to do so. Such behavior is a product of a specific altercation in the cells’ section of genetic code responsible for producing a protein called “AKT1 kinase”, which is specifically designated to regulating cell proliferation, cell differentiation, and apoptosis among other additional functions involving the nervous system.…

    • 658 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    Pancreatic Cancer Essay

    • 1222 Words
    • 5 Pages

    DNA mutations can turn on oncogenes or turn off tumor suppressor genes. Gene mutations are usually inherited, therefore it is always important to watch out for diseases that are present in family…

    • 1222 Words
    • 5 Pages
    Superior Essays
  • Improved Essays

    CRISPR-Cas9 system: new perspectives to cancer treatment Genetic interactions screens are used to detect genetic interactions and, as a result, to provide information into the functions of each gene and their associations with other components in the cell [2]. A genetic interaction is defined as when two genes interact and generate a phenotype that was not expected in light of each of the gene’s effect [1]. In mammalian cells, most of the genetic interaction assays use RNA interference (RNAi) techniques [3], which is method of silencing a gene based in the degradation of specific messenger RNA (mRNA) molecules. Described initially in plants, RNA interference was also observed in most of the eukaryotic organisms, such as insects, mice, and humans.…

    • 1127 Words
    • 5 Pages
    Improved Essays
  • Superior Essays

    This new finding could not be compared to structural data of NRSF because none is currently available. They found genes encoding 110 transcription factors, 22 microRNAs, and 5 slicing regulators all associated with NRSF. This proposes a possible negative autoregulatory feedback mechanism. For the first time, they…

    • 1258 Words
    • 6 Pages
    Superior Essays
  • Superior Essays

    Hereditary Cancer Cancer is one of the most unknown subjects in the medical world. When it comes, why it comes, and how to effectively contain it is still being studied. Treatments have been available to lessen the cancer, or in some cases, take it away. The medical community has come so far in our knowledge of cancer. Splitting cancer into two specific groups of somatic cancer and hereditary cancer, researchers are getting more information.…

    • 1357 Words
    • 6 Pages
    Superior Essays