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Question F5
Excited by the discovery of this novel cancer driver, researchers aimed to develop a therapeutic approach to target MFAB.Which cancer therapeutic approach would most effectively target this mutated protein to help limit cancer progression? What impact would this have on the action of MFAB and how would you test the safety and efficacy of this novel therapeutic?
4 marks
Question F2
To better understand the impacts of this MFAB mutation on cancer progression, pathologists performed an immunoblot on Mr Jones’ tumour biopsy, in order to assess changes in cellular signalling pathways. This was analysed alongside healthy intestinal tissue. Actin served as a loading control, ensuring equal protein was loaded.
3 marks
Question F4
Further testing revealed that Mr Jones' adenocarcinoma had spread to other sites in the body. Describe the molecular and cellular changes that facilitate this process.
4 marks
Question F3
Which other cell types within the tumour microenvironment would help to promote the cancer hallmark identified in B? In your answer be sure to describe the role of these cell types in contributing to this hallmark.
5 marks
Question F1
Using the information provided, determine the type of change this mutation causes in the encoded amino acid at position 505. Given this change, what is the likely impact of this mutation on MFAB function and how would you classify this type of cancer mutation?
4 marks
Part I What is the normal function of HER2 and how does it contribute to cancer development?
Part II Give three differences between “A” and “B” pathways.
Question 3
Which of the figures (A or B) is most likely to be associated to Ms Mayo and why?
Question 2
With regards to (i) angiogenic switch, and (ii) metastasis, what will be the cellular outcome of cells from (A) and (B) pathways?
Which statement about retinoblastoma is CORRECT?
Identify which gene type does NOT contribute to human cancer: