Great Deal! Get Instant $10 FREE in Account on First Order + 10% Cashback on Every Order Order Now

Identification of biomarkers of prostate cancer using regression analysis Bivariate regression analysis is a quick and simple method for the Identification of the importance of biomarkers for gene...

1 answer below »
Identification of biomarkers of prostate cancer using regression analysis
Bivariate regression analysis is a quick and simple method for the Identification of the importance of biomarkers for gene expression a
ays with respect to a given question. By regressing the gene expression profile of one sample against another sample of a different type we can measure the similarity and difference in expression of all the genes on the a
ay. This is achieved by conducting a regression analysis and recording the standard residual values for each gene. The higher the standard residual value the more significant the difference in expression. A negative standard residual means down regulation with respect to control and positive regulation. A standard residual of greater than 2 is significant. By ranking the standard residual values, we can identify the most important genes. Here we use this technique for a set of prostate cancer cases with matched control cases.
Aims
1. To utilise regression analysis to analyse gene expression a
ay data.
2. To identify genes associated with prostate cancer.
3. To review the known roles of these genes in the context of cancer.
ASSESSMENT (Overview of Assignment)
ABSTRACT (≤ 300 words)
· Provide a 300 word abstract that summarises the study.
· Include Background, Approach, Results, Conclusions.
· Look at examples of abstracts from microa
ay studies and try and emulate this here.
RESULTS AND ANALYSIS
· Include clear supportive commentary that sets the scene for the analysis performed.
· A clear summary table of data that defines the top 5 overexpressed genes and the top 5 under expressed genes. Where possible provide additional detail to this summary table.
Provide supportive commentary that describes the main findings.
· Make use of pathway analysis tools (http:
www.reactome.org/) using the identified genes mention the pathways that are associated with top 5 overexpressed genes and the top 5 under expressed genes in the form of table. Give supportive commentary under the table.
Below mentioned are the top 5 overexpressed genes and the top 5 under expressed genes
· Make the use of genemania and input each of the top 20 and bottom 20 genes from the microa
ay study. This will produce a gene interaction network. Then select any 2 genes other than the top 5 overexpressed genes and the top 5 under expressed genes that are highly expressed in the gene interaction network. And mention about their role in prostate cancer and explain why you choose that 2 gene. Present the data in an appropriate figure (gene interaction network)
Below mentioned are the top 20 overexpressed genes and the bottom 20 under expressed genes
· Make use of Protein Atlas database. Include an overview table figure.
Input each of the top 5 overexpressed genes and the top 5 under expressed genes from the microa
ay study.
e.g. Headers that you could use include:
TISSUE TYPE: Gene name, Tissue with highest protein expression, Protein expression level in Prostate
CELLULAR: Main cellular location, Expression in prostate cell lines (RNA expression overview)
PATHOLOGY: % expression in patients with prostate cancer.
DISCUSSION (≤ 1000 words)
· Interpret the results by assessing the link between the differentially expressed genes and prostate cancer.
· Association of the target genes with prostate cancer or mechanisms associated with tumor proliferation, survival, metastasis, etc.
· Consider and define how further validation of the differentially expressed genes could be conducted.
· Identify appropriate methods to further investigate how the proteome from control and tumour tissue could differ. How could the results from the cDNA microa
ay experiment be linked to the changes that may occur in the proteome.
· Appropriate use of the literature.
· Review the genes discovered in the context of cancer. Make use of the databases (e.g. Genecards, Ensemble, NCBI, UniProt etc). Also paste into PubMed, Science Direct, Google scholar, etc) to find articles and information that relates to the role of the gene in prostate cancer and pathways linked to cancer.
CONCLUSIONS
· Interpretation.
· Clear points that summarise the findings.
REFERENCES
· Co
ect citation.
· Appropriate Harvard referencing.
Marking grid
Abstract
Clear, relevant & contextualized aims / objectives
The approach is accurate and utilizes relevant information that aligns with the topics under investigation.
Exceptional knowledge and understanding of the area of study that considers
elates all relevant information.
Work is of an exceptional standard and draws on material beyond the prescribed range.
Results & analysis
Exceptional demonstration of analysis skills producing high quality work
Exceptional handling of data analysis.
Accurate / defined regression analysis examples with collated data tables.
Excellent and appropriate presentation of data (e.g. tables figures with comprehensive titles and legends).
Results are described concisely and appropriately and reflect the data presented. Work is of an excellent standard with strong scientific writing evident.
Discussion, Interpretation & Conclusion
Logical and detailed interpretation of the data supported by critical evaluation/ synthesis/ analysis and evidenced with appropriate references.
Work is of an excellent standard with strong scientific writing evident and drawing on material beyond the prescribed range
Resources/ References & Overall Presentation
References are relevant and cu
ent and are cited appropriately. Presentation is of a professional standard.
Performance in all areas deemed beyond expectation of the level and the prescribed range.
Answered Same Day Feb 13, 2021

Solution

Steve answered on Feb 15 2021
152 Votes
USE OF REGRESSION ANALYSIS TO IDENTIFY PROSTATE CANCER BIOMARKERS
STUDENT NAME:
COURSE NAME:
PROFESSOR NAME:
UNIVERSITY AFFILIATIONS:
STATE:
DATE
Table of Contents
ABSTRACT    3
RESULTS AND ANALYSIS    4
DISCUSSION    5
CONCLUSIONS    9
REFERENCES………………………………………………………………………………………………………………………………………….10
USE OF REGRESSION ANALYSIS TO IDENTIFY PROSTATE CANCER BIOMARKERS
ABSTRACT
Background: Most of the deaths in men was Prostate cancer which became fifth in rank of cancer type of infection that caused a high number of deaths in males. The physicians have experienced immense difficulties in being in a position to understand the treatment response of Prostate cancer for them to be in a position to cu
overtreatment and minimize the mortality rate caused by prostate cancer by getting to know the affected patients and exactly when to treat them for full recovery (Shao et al., 2009, pg.1280-1283).
Approach: Presently, the decision for treatment of Prostate cancer and its prognosis involved Gleason score which entails the subsequent biopsies for histopathological staging, prostate-specific antigens, and digital rectal examination. These procedures are highly significant although they have their deficiency. There are commitments that are cu
ently exercised to ensure better and effective non-invasive and clinically meaningful biomarkers being developed linking nucleic acids, proteins, omics approaches and circulating tumor cells.
Results: Prostate cancer biomarkers will most probably be a test engaging several biomarkers in combination by using gene microa
ays and protein. They comprise of markers that are repressed in prostate cancer differently. The damage of DNA response genes adversely affects healthy genome maintenance. Deficiencies in DNA repair genes and cell cycle ba
ier usually abe
ant downregulation or mutation lead to a lot of human diseases such as cancer and growth of neurodegenerative conditions. Mutations that are inherited in specific genes such as BRCA2, HOXB13 and BRCA1 lead to hereditary cases of prostate cancer. Most of the men with alterations in the above genes are usually at a higher risk of being infected by prostate cancer among other categories of cancers during their lifespans.
Conclusions: The results have significant impacts for the discovery of cancer biomarker in the enlargement of specimen e
or unaffected clinical biopsy assessment for the estimation of the assertiveness of prostate cancer.
RESULTS AND ANALYSIS
The data below represents the analysis performed by the use of genemania to represent the highest five ove
epressed genes and under-repressed genes respectively;
Figure 1:
    Over repressed Genes
    Under repressed genes
    PCA3
    ASPssedd
    C1QTNF3-AMACR
    CYP4B1
    DLX1
    CYP3A5
    OR51E2
    SERPINB11
    ZIC2
    PDE1C
    MS4A8
    NDUFA4
    C15orf48
    GLYATL1P3
The MS4A8 and C15orf48 are over repressed genes that did not show strong moderation to the cytoplasmic positivity. Prostate cancer was in generally negative in these genes. On the other hand, NDUFA4 and GLYATL1P3 are under repressed genes that showed strong moderation to cytoplasmic positivity. The figs below are the networks of both the 20 over repressed genes and the 20 under repressed genes.
Under repressed genes, source: genemania
Over repressed genes source: genemania
DISCUSSION
Next-generation sequencing and microa
ays are genomic technologies that have greatly enhanced the cohort of molecular autographs for prostate cancer. The list of genes that are repressed differentially between non-malignant and malignant states have been thought to putative prostate cancer biomarkers sources that are productive. Nevertheless, the highly variable due to different reasons. The use of genome sequencing data of the next generation from non-malignant...
SOLUTION.PDF

Answer To This Question Is Available To Download

Related Questions & Answers

More Questions »

Submit New Assignment

Copy and Paste Your Assignment Here