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Sequencing suggests a shared blood supply carried one twin's sarcoma to her sister

Sanger Institute researchers sequenced 45 samples from one pair of twins and found that a rare sarcoma began in one sister and spread to the other before birth. The same genomes hint at a different way for identical twins to form, though this is one pregnancy.

The Scientist · Science desk

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Illustration accompanying Sequencing suggests a shared blood supply carried one twin's sarcoma to her sister
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Twin A's sarcoma cells formed twin B's tumours How the sarcoma began in one twin and reached the other. The story's two numbers make no single point, so this is drawn as a map.

Twin A: a gene fusion late in the first trimester led to sarcomas in her face, brain and liver. Twin B: her skin and brain tumours were twin A's cells, arriving late in the second trimester. Behjati: likely via shared circulation, from one crossed cell. Findings rest on one twin pair.

Twin A's sarcoma cells formed twin B's tumours
WhoHowKindClaim
Twin AMN1-ZNF341 gene fusion near the end of the first trimester led to sarcomas in her face, brain and liverexposure6
Twin BTwin A's tumour cells reached her near the end of the second trimester, forming her skin and brain tumoursexposure7
Shared circulationBehjati says the cancer probably spread through the twins' shared circulationexposure8
Twin B's tumourPer Behjati, it appears to have formed from one cancer cell from twin A that crossed over and multipliedexposure10
The evidenceFindings on the cancer's spread and the embryo's split rest on a single twin pairconstraint16

What happened

  • The twins, Amelia and Amaya, were delivered by caesarean section at 34 weeks after a scan showed a facial mass on one of them.
  • A fusion of the genes MN1 and ZNF341 arose in twin A around the end of the first trimester, for unknown reasons, and produced soft tissue sarcomas.
  • Around the end of the second trimester, twin A's tumour cells reached twin B, whose skin and brain tumours were made of those cells.

Why it matters

  • constraint Every statement about how these twins formed rests on one pregnancy, so the data cannot yet say how common a single-cell origin is.
  • capability Mutations that build up after separation let researchers tell two genetically matched sisters apart and date when a tumour began and when it crossed.
  • exposure Twins who share a placenta share blood vessels, so cells have a route between them, though Behjati calls cancer in a newborn extraordinarily rare.
  • decision The Sanger team has chosen to study twinning systematically, and that larger sample will show whether a one-cell origin recurs.

Identical twins make a tidy experiment because they start with matching DNA. After the embryo separates, each twin collects its own small mutations, and those differences let researchers tell the sisters' cells apart and estimate when events happened [5]. The team applied that to 45 post-mortem samples from organs, placenta and tumours [4]. The dates are estimates; the report words them as "around" the end of each trimester [6][7].

The question going in was whether the cancer arose once and spread, or arose twice, perhaps from a shared inherited mutation [3]. Twin B's skin and brain tumours were made of twin A's tumour cells [7]. The MN1-ZNF341 fusion arose in twin A, for reasons the researchers could not identify [6].

The route is plausible on anatomy. Behjati said the cancer probably spread through the twins' shared circulation [8]. "When you share a placenta, you inevitably end up sharing blood vessels," he said [9]. By his account, the tumour in twin B appears to have grown from a single cell that crossed over and multiplied [10].

The embryo finding is the stranger result. The long-held picture is an embryo splitting in half, with half the cells going to each twin [11]. In these sisters, one cell became twin A, and every other cell became twin B and the entire placenta [12]. Behjati said the placenta is where researchers would take notice: "If you go to placenta researchers and say, 'Here's this pregnancy where one twin made all the placenta', they're going to say, 'Oh, that's interesting'," he said [13].

Everything here comes from one pair [16]. New Scientist's report says the analysis led to a "radical rethink" of how identical twins split apart [17], but a single pregnancy can only establish that a split like this happens. The study cannot say how common a one-cell origin is, or whether twins who do not share a circulation ever form this way.

The team intends to find out. Behjati said they are setting up a study to "look into twinning more systematically, because the questions this raises are really quite fascinating" [14].

What to watch

  • Results from the systematic twinning study Behjati's team is setting up, and whether other shared-placenta pregnancies show one twin supplying the whole placenta.
  • Whether a second case of cancer crossing between twins in the womb is documented with the same sequencing approach.
  • Publication details for the sisters' study, including how the single-cell origin was established from the placental samples.

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What the record supports and how the coverage leans. The claims behind it follow.

Reality

Evidence55
Adoption
Insufficient
Hype gap+30
Incentives
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Confidence45
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  1. [1]

    The twins, Amelia and Amaya, were delivered by caesarean section at 34 weeks' gestation after one was found to have a facial mass during a scan.

    Reported SupportedView cited source
  2. [2]

    When born, both twins were found to have cancer in multiple locations, and they died soon afterwards.

    Reported SupportedView cited source
  3. [3]

    The question was whether the cancer arose in one twin and spread to the other, or developed separately, perhaps due to a shared inherited mutation that predisposed both to the condition.

    Reported SupportedView cited source

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Sources

1 independent publisher whose own reporting we read for this story.

  1. newscientist.com

    1 article · October 14, 2026

    Rare cancer spread between twins in utero

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