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University of Exeter Medical School

Molecular Pathology of Cancer and Application in Cancer Diagnosis, Screening and Treatment ONLINE

Module titleMolecular Pathology of Cancer and Application in Cancer Diagnosis, Screening and Treatment ONLINE
Module codeHPDM038Z
Academic year2021/2
Credits15
Module staff

Dr Vikki Moye (Convenor)

Duration: Term123
Duration: Weeks

8

Number students taking module (anticipated)

40

Module description

This module will equip you with detailed knowledge and understanding of the molecular mechanisms involved in cancer development. This will include the ways in which interrogation of a person’s own genome, and the genome of tumour cells, can facilitate the diagnosis and treatment of cancer.

Module aims - intentions of the module

This module covers the molecular mechanisms that underlie cancer development, growth and metastasis, and the differences between different cancers. It will explore the different molecular and cellular actions of anti-cancer treatments, the genomic factors affecting response and resistance to treatment, and the research approaches to anti-cancer drug design and development. Broad situations which confer a high cancer risk to a person and/or to other members of the same family will be discussed in the context of how genomic information may be integrated into cancer screening programmes. This module will prepare you to interrogate the cancer data sets from the ‘100,000 Genomes Project’ if relevant for your research project.

Intended Learning Outcomes (ILOs)

ILO: Module-specific skills

On successfully completing the module you will be able to...

  • 1. Analyse the molecular and cellular processes leading to cancer development and emerging changes in tumour classification
  • 2. Appraise the genomic basis of cancer predisposition, and how this is used to identify people and families at higher risk of cancer
  • 3. Critically evaluate how genomic information is currently applied in the diagnosis, classification, prognosis treatment selection and monitoring of cancer (e.g. leukaemia, breast cancer, melanoma, lung cancer).
  • 4. Analyse how information from genome analysis of neoplastic cells, and RNA sequencing data, can be used to investigate the molecular and cellular processes leading to cancer development and inform strategies for drug development.

ILO: Discipline-specific skills

On successfully completing the module you will be able to...

  • 5. Describe in detail the role of tumour suppressor genes and oncogenes in the development of cancer.
  • 6. Explain and summarise the eight ‘hallmarks’ of cancer.

ILO: Personal and key skills

On successfully completing the module you will be able to...

  • 7. Critically reflect on personal practice and make connections between known and unknown areas, to allow for personal development, adaptation and change.
  • 8. Respond to innovation and new technologies and be able to evaluate these in the context of best practice and the need for improved service delivery.
  • 9. Communicate accurately and effectively with peers, tutors and the public.

Syllabus plan

Whilst the module's precise content may vary from year to year, an example of an overall structure is as follows:

  • Cellular properties of tumours: growth, division, invasion, aberrant hormone or toxin production, immunogenicity including T cell and B cell repertoire profiling
  • Tumour classification systems
  • Factors in tumour formation: molecular mechanisms and role of microenvironment, molecular signatures & changing classification
  • Diagnosis, molecular sub-classification, aggressiveness (prognosis) characterisation of metastases
  • Breakthrough tumour /metastases and molecular mechanisms
  • Genomic testing of solid tumours and haematological cancers
  • Analytical and interpretation challenges in genomics as applied to cancer
  • Genomic and cellular markers and optimal treatment regimes in haematological cancer and solid tumours
  • Monitoring disease following treatment (medical, surgical or bone marrow transplant)
  • Molecular basis of germline mutations for cancer predisposition
  • Approaches to identify new genes and susceptibility loci: GWAS studies; other predisposition biomarkers
  • Environmental factor and lifestyle predisposition and protection; molecular action; genomic interaction; epigenetic factors
  • Role of genomics in drug development and the role of clinical trials as part of treatment options

Learning activities and teaching methods (given in hours of study time)

Scheduled Learning and Teaching ActivitiesGuided independent studyPlacement / study abroad
01500

Details of learning activities and teaching methods

CategoryHours of study timeDescription
Guided independent study10Tutor guided online discussion forum
Guided independent study15Preparation of e-FlashCards (for formative and summative assessment)
Guided independent study20Writing essay
Guided independent study105Online resources and independent guided literature research

Formative assessment

Form of assessmentSize of the assessment (eg length / duration)ILOs assessedFeedback method
Formative E-flashcard1 hour1-6,9Oral
Participation in online discussion Weekly1-9Written

Summative assessment (% of credit)

CourseworkWritten examsPractical exams
10000

Details of summative assessment

Form of assessment% of creditSize of the assessment (eg length / duration)ILOs assessedFeedback method
E-Flashcard 1206 PowerPoint slides maximum (per flash card)1-6, 9Written/Oral
E-Flashcard 2206 PowerPoint slides maximum (per flash card)1-6, 9Written/Oral
Essay602000 words1-9Written
0
0
0

Details of re-assessment (where required by referral or deferral)

Original form of assessmentForm of re-assessmentILOs re-assessedTimescale for re-assessment
E-flashcard 1 (20%)E-flashcard 1 (6 PowerPoint slides maximum (per flash card))1-6, 9Typically within six weeks of the result
E-Flashcard 2 (20%)E-flashcard 2 (6 PowerPoint slides maximum (per flash card))1-6, 9Typically within six weeks of the result
Essay (60%)Essay (2000 words)1-9Typically within six weeks of the result

Re-assessment notes

Please refer to the TQA section on Referral/Deferral: http://as.exeter.ac.uk/academic-policy-standards/tqa-manual/aph/consequenceoffailure/

Indicative learning resources - Basic reading

  • Weinberg, R. (2014). The biology of cancer . New York: Garland Science.
  • Read, A. and Donnai, D. (2015). New clinical genetics. Bloxham, Oxfordshire: Scion.
  • Turnpenny, P. and Ellard, S. (2012). Emery's elements of medical genetics. Philadelphia: Elsevier/Churchill Livingstone. (electronic access through University of Exeter library)
  • Strachan, T., Read, A. and Strachan, T. (2011). Human molecular genetics 4 . New York: Garland Science.
  • Strachan, T., Goodship, J. and Chinnery, P. (2015). Genetics and genomics in medicine. New York: Garland Science.

Indicative learning resources - Web based and electronic resources

http://vle.exeter.ac.uk/course/view.php?id=6142

 

Henry Stewart Talks Cancer Genetics:

 

https://hstalks.com/playlist/941/cancer-genetics/?biosci

Key words search

Tumour, cancer, diagnosis, classification, treatment, risk

Credit value15
Module ECTS

7.5

Module pre-requisites

N/A

Module co-requisites

N/A

NQF level (module)

7

Available as distance learning?

No

Origin date

01/12/2015

Last revision date

13/07/2020