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Assessing the Role of Hypoxia in Cancer Treatment Resistance and Prognosis Assignment Sample

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MRI as a Potential Biomarker for Assessing Tumor Hypoxia: Opportunities and Challenges

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Hypoxia is hypothesized to contribute to some chemotherapy and radiotherapeutic antibiotic resistance and is regarded as a key prognostic factor for solid tumors. Tumor hypoxia is a powerful predictive marker for disease progression, metastasis development, and overall patient survival. This research investigation was completed after methodology formulation and critical evaluation. MRI offers a number of benefits as a prognostic, diagnostic, response biomarker, and predictive with the capacity to perform various contrast and imaging at a multiparametric quantitative level. The early glycemia profile with hypoxia has been connected to a distinctive pattern of brain irregularity using MRI.


MRI is currently thought to be the best non-invasive biomarker and has been used to treat a variety of illnesses, including hypoxia. The search for trustworthy biomarkers continues to be a high goal in the medical community. The main objective of the physicians has been connected to hypoxia and tumors: to assess the severity of the hypoxic tumors in order to apply various therapeutic modalities. In order to comprehend hypoxia, it is vital to routinely carry out a variety of therapy methods that combine the crucial knowledge regarding oxygenation incorporation. Tissue-level hypoxia is one of the key characteristics of many important patient morbidities and mortality causes.

Testing your Case

The researcher will find it easier to analyze the data, and mapping the determined values will be simple to complete. Incorporating this data analysis procedure, it not only benefits the study execution but also makes it easier for the individual to address needs in an acceptable manner. The chosen methodological technique will be able to illustrate the mean values that are present in response to 100% FiO2 readings while also offering a suitable supportive environment (Chalak et al. 2018). The researcher will be able to quickly execute the average percentage changes measurement that is obvious in R1.

Proposed Solution

Biomarkers must be technically sound, demonstrated to detect tumor biology, and linked to clinical outcomes in order to be used to evaluate hypoxia. The capability to directly observe oxygenation in tumors using the “needle electrodes” was important in verifying the connections between treatment responses and hypoxia using “Eppendorf histography”. This procedure isn't basically obtainable; it was effective only on tumors which were accessible easily. Pre-clinical tests often evaluate “tissue-level hypoxia”, but it can be also likely to map the geographic distribution of “hypoxic tumor tissue” in people (Nair, 2018). Also, there are techniques that operate exogenously supplied substances, like nitroimidazoles, that bind to macromolecules in cells while they are hypoxic. Alternative methods make use of hypoxia-related gene signatures.


Because it offers a variety of independent contrast mechanisms that look at different elements of hypoxia, MRI is intriguing. The majority of this information is based on rat tumor models, and further studies are required to build on the few small studies that have already been conducted to make sure that these findings are applicable to a range of human cancer types. Technical validation has also received some research attention. Despite the fact that these outcomes are encouraging, further proof is required to confirm high-to-excellent repeatability in a multicenter setting.

Reference list


  • Abassi, Z., Rosen, S., Lamothe, S. and Heyman, S.N., 2019. Why have detection, understanding and management of kidney hypoxic injury lagged behind those for the heart?. Journal of Clinical Medicine, 8(2), p.267.
  • Chalak, L., Latremouille, S., Mir, I., Sánchez, P.J. and Sant'Anna, G., 2018. A review of the conundrum of mild hypoxic-ischemic encephalopathy: current challenges and moving forward. Early human development, 120, pp.88-94.
  • Nair, J. and Kumar, V.H., 2018. Current and emerging therapies in the management of hypoxic ischemic encephalopathy in neonates. Children, 5(7), p.99.
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