Questions and answers

Is cancer hereditary?

The difference between hereditary, familial and sporadic cancer, and who should have genetic counselling and testing

Updated: 28 October 20262 min read7 references
Short answer

Cancer itself is not passed from parents to children, but some gene changes that raise the risk of cancer (such as mutations in the BRCA1 and BRCA2 genes) can be inherited [1]. Only about 5 to 10 per cent of cancers are hereditary. The rest come from gene changes that happen during life, with ageing, tobacco smoke, radiation and other factors [2, 3]. Having an inherited mutation means a higher risk, not that you will definitely get cancer [1].

Key points

  • In a study of more than 10,000 patients with 33 types of cancer, fewer than 1 in 10 had a related inherited mutation [4].
  • Having no family history does not mean you are not at risk; about 4 in 10 people develop cancer during their lifetime [3].

Hereditary, familial or sporadic?

The gene changes that lead to cancer arise in three ways [1]:

  • Random mistakes when cells divide
  • Damage to DNA from outside factors, such as tobacco smoke, sunlight and the HPV virus
  • Inheritance from the father or mother

Most cancers come from random changes building up over the years [1].

Hereditary cancer is uncommon: family members have a higher risk of one or more cancers because of an inherited gene mutation and sometimes develop cancer at a young age. For example, in an inherited bowel condition (FAP), the chance of bowel cancer at a young age is very high [1]. But not every cancer that "runs in the family" is hereditary; shared lifestyles and habits, chance (especially with common cancers such as prostate cancer) or several small gene changes can also be the cause [1].

In a large study of twins, genes explained about a third of the difference in cancer risk between people; this share was higher in melanoma and prostate cancer (more than half) and about a third in breast cancer [6].

Diagram of a cell and its nucleus containing the chromosomes
Genes sit on chromosomes in the nucleus of every cell. Most cancers arise from gene changes that happen during life; only a small share (about 5 to 10 per cent) is due to an inherited mutation such as BRCA.Image: Cancer Research UK · CC BY-SA 4.0 · Wikimedia Commons (adapted: Persian labels)
Out of every 10 women with a BRCA mutation, how many get this cancer by age 80? [5]
GeneBreast cancerOvarian cancerCancer in the other breast (within 20 years)
BRCA1About 74 to 54
BRCA2About 71 to 22 to 3

The risk changes with the number of affected relatives and where the mutation is in the gene [5].

Which signs suggest hereditary cancer?

According to the US National Cancer Institute, these signs make hereditary cancer more likely, and it is worth talking to your doctor about genetic counselling [2]:

  • A family member has a known inherited mutation
  • Cancer at a young age (for example bowel cancer before age 50)
  • Several types of cancer in one person
  • Several family members, especially first-degree relatives, with the same type of cancer; or breast and ovarian cancer, or bowel and womb cancer, in the same family
  • Cancer in both breasts or both kidneys
  • Rare cancers, such as breast cancer in a man

Guidelines recommend genetic testing for everyone with these cancers: triple-negative breast cancer, ovarian cancer, pancreatic cancer, bowel cancer before age 50, prostate cancer that has spread, and breast cancer in a man [2].

What should I do if cancer runs in my family?

Talk to your doctor or a genetic counsellor about your family history. It is best for testing to start with a family member who has had cancer [2]. "Home" genetic tests have major limitations and are not recommended for assessing inherited risk [1].

For bowel cancer: if your father, mother, sister, brother or child had bowel cancer or an advanced polyp before age 60 (or two of them at any age), a colonoscopy every 5 years is recommended from age 40, or 10 years before the age of the youngest affected relative, whichever is earlier [7]. For stomach cancer: if someone in your family has had stomach cancer, get tested for Helicobacter (read more).

Related questions

If my father or mother had cancer, will I definitely get it?

No. Only about 5 to 10 per cent of cancers are hereditary [3], and even having a high-risk mutation means a higher risk, not certain illness [1].

How is an inherited genetic test different from a tumour gene test?

An inherited test is usually done on blood or saliva and shows mutations passed on from your parents. A tumour test shows changes that have arisen in the cancer cells themselves and is used to choose medicines. A tumour test sometimes also reveals an inherited mutation, but it does not replace an inherited test [2].

How long do genetic test results take?

Usually about 2 to 3 weeks [2].

References

7 references
Show all references, 4 with a study cardClose the reference list

Numbers in the text, such as [1], refer to these sources. Sources with a “Study card” button are summarised in the site’s evidence library.

  1. 1
    The Genetics of CancerNational Cancer Institute · cancer.gov · 2024
    Source Back to text: 1 2 3 4 5 6 7 8
  2. 2
    Genetic Testing for Inherited Cancer RiskNational Cancer Institute · cancer.gov · 2024
    Source Back to text: 1 2 3 4 5 6
  3. 3
    Common Cancer Myths and MisconceptionsNational Cancer Institute · cancer.gov · 2024
    Source Back to text: 1 2 3
  4. 4
    Pathogenic Germline Variants in 10,389 Adult CancersHuang KL, Mashl RJ, Wu Y, Ritter DI, Wang J, Oh C, et al · Cell · 2018;173:355-370.e14
  5. 5
    Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation CarriersKuchenbaecker KB, Hopper JL, Barnes DR, Phillips KA, Mooij TM, Roos-Blom MJ, et al · JAMA · 2017;317:2402
    Study cardDOIPubMed Back to text: 1 2
  6. 6
    Familial Risk and Heritability of Cancer Among Twins in Nordic CountriesMucci LA, Hjelmborg JB, Harris JR, Czene K, Havelick DJ, Scheike T, et al · JAMA · 2016;315:68
  7. 7
    Colorectal Cancer Screening: Recommendations for Physicians and Patients From the U.S. Multi-Society Task Force on Colorectal CancerRex DK, Boland CR, Dominitz JA, Giardiello FM, Johnson DA, Kaltenbach T, et al · Gastroenterology · 2017;153:307-323

This page is based on reputable scientific sources and was last updated on 28 October 2026. The content of this website is for educational and informational purposes only and does not replace consultation, diagnosis or treatment by a specialist physician. Consult your treating physician about any treatment decision.