Gene expression and cancer (A-level only)

    AQA
    A-Level

    A tumour is a mass of cells produced by uncontrolled mitosis. Benign and malignant tumours differ in ways you can be asked to compare. Benign tumours grow slowly and remain compact, usually surrounded by a capsule of fibrous tissue. Their cells are differentiated, resembling normal cells with normal-sized nuclei. Because they do not invade, surgical removal is usually a permanent cure. They can cause harm by pressing on an organ, causing blockages, or releasing excess hormones. Malignant tumours grow rapidly, are irregular in shape and lack a capsule, so they invade surrounding tissue. Their cells are undifferentiated, with large, dark nuclei, and can spread (metastasise).

    6
    Objectives
    6
    Exam Tips
    8
    Pitfalls
    12
    Key Terms
    10
    Mark Points

    Subtopics in this area

    The main characteristics of benign and malignant tumours.
    The role of the following in the development of tumours: tumour suppressor genes and oncogenes abnormal methylation of tumour suppressor genes and oncogenes increased oestrogen concentrations in the development of some breast cancers.

    Gene expression and cancer (A-level only) Revision Guide

    Learning Objectives

    What you need to know and understand

    • Compare benign and malignant tumours using growth rate, capsule, differentiation and ability to spread.
    • Explain why metastasis makes a malignant tumour far harder to treat than a benign one of the same size.
    • Identify, from a description or micrograph, whether a tumour is likely to be benign or malignant and justify the choice.
    • Explain how a single mutation in a proto-oncogene produces a protein that drives division without a growth factor.
    • Describe two different ways, one genetic and one epigenetic, in which a tumour suppressor gene can stop producing its protein.
    • Suggest how a raised oestrogen concentration increases the rate of mitosis in breast tissue, referring to transcriptional factors.

    Marking Points

    Key points examiners look for in your answers

    • one mark for a benign tumour growing slowly and a malignant tumour growing rapidly, both by uncontrolled mitosis
    • one mark for benign cells being differentiated, while malignant cells are undifferentiated with large, dark nuclei
    • one mark for the benign tumour being surrounded by a capsule so it stays in one place and does not invade surrounding tissue
    • one mark for malignant cells breaking off and spreading in the blood or lymph to form secondary tumours, that is metastasis
    • one mark for benign tumours usually being cured by removal whereas malignant tumours frequently recur
    • one mark for a mutation converting a proto-oncogene into an oncogene whose protein is permanently active or overproduced
    • one mark for the outcome being rapid or uncontrollable cell division
    • one mark for a mutated or hypermethylated tumour suppressor gene producing no protein or a non-functional protein, so the cell cycle is not stopped
    • one mark for increased methylation of DNA inhibiting transcription, and decreased methylation stimulating transcription
    • one mark for increased oestrogen concentration stimulating transcription of genes that drive mitosis in breast tissue

    Examiner Tips

    Expert advice for maximising your marks

    • ๐Ÿ’กAnswer comparison questions in pairs: name the feature, then give both tumour types in the same sentence.
    • ๐Ÿ’กUse the terms differentiated, capsule and metastasis when comparing tumour types.
    • ๐Ÿ’กIf the question gives a micrograph, comment on nucleus size and cell shape rather than guessing from the caption.
    • ๐Ÿ’กBoth routes end in the same outcome - rapid or uncontrollable cell division - so make that your final point.
    • ๐Ÿ’กDecide first whether the question is about a mutation or about methylation, as the mechanisms differ.
    • ๐Ÿ’กWhen discussing oestrogen, mention that it can stimulate transcription of genes that lead to cell division.

    Common Mistakes

    Pitfalls to avoid in your exam answers

    • stating that benign tumours are harmless, when they can compress an organ, cause blockages or secrete excess hormone
    • saying benign tumours 'are not cancerous' without giving a structural or behavioural difference
    • describing spread vaguely as 'moving through the body' without naming the blood or lymph
    • writing that tumour cells divide by meiosis rather than mitosis
    • writing that the oncogene produces no protein or a non-functional protein, when an oncogene's product is overactive or overproduced
    • reversing the methylation directions and stating that tumour suppressor genes are hypomethylated in cancer
    • answering 'growth' instead of cell division or mitosis
    • saying meiosis rather than mitosis when describing the division of tumour cells