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A Cancer That Crossed From One Twin to Her Sister in the Womb

By Jeff Paroddy · · 3 min read · Facts first

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Topics: Offbeat

Ink and neon drawing of a glowing tree of blood vessels linking two softly glowing spheres, with one tiny bright red cell travelling along a vessel from one to the other
Illustration: Jeff Paroddy

Jeff's Daily Pick. Two identical sisters were born with the same rare cancer. Their DNA shows it started in one twin and crossed to the other through the placenta.

In the United Kingdom, researchers at the Wellcome Sanger Institute, Great Ormond Street Hospital and the University of Cambridge reconstructed how a rare cancer reached two identical twin girls before birth. The study, published on October 6, 2026 in Nature Communications, shows the tumor began in one sister and spread to the other through the placenta they shared. Both children died shortly after birth, and their mother asked that the work be dedicated to them.

The case

A fetal MRI at 33 weeks showed a mass on the face of one twin, which prompted early delivery a week later. At birth, tumors were found in both girls. The cancer was an undifferentiated sarcoma, a soft tissue tumor driven by a rare gene fusion, MN1::ZNF341. The question was whether it had arisen twice, from something both twins shared, or once.

Reading the family tree

Identical twins start from one fertilized egg, but each cell picks up small DNA changes as it divides, which leave a lineage record. The team sequenced 10 tumor samples, 12 normal tissue samples from the twins, 11 placental samples and 12 placental samples enriched for cells that build the placenta. Every tumor sample from both girls carried the genetic signature of twin A. The cancer started in her, likely near the end of the first trimester, and crossed to twin B in a single transfer late in the second trimester. Twin B's tumors appear to descend from one cell. Those dates depend on an assumed mutation rate and are estimates.

The analysis turned up two more surprises. Normal blood cells moved the other way: about 75% of the cells in a spleen sample from twin A came from twin B. And the earliest cell lineages contributed unevenly, one branch mostly to twin A, another to both girls and the placenta, so the embryo did not split evenly.

What it shows / what it doesn't

  • Shows: in this case, the sarcoma originated in one twin and was transmitted to the other before birth, most likely through shared placental blood vessels.
  • Shows: DNA lineage tracing can date and orient events in early development.
  • Doesn't show: the cells crossing directly; the route is inferred from genetics.
  • Doesn't show: that cancer often passes between twins. This was an extremely rare event, one case.
  • Status: peer reviewed single family study with research autopsy consent.

Twin to twin transfer of leukemia has been documented before through shared placental circulation. This is a solid tumor, traced cell by cell. Study author Sam Behjati told New Scientist that sharing a placenta inevitably means sharing blood vessels. The method, the authors note, can be reused to study how other childhood cancers begin.

Sources

Peer reviewed case study

Embryonic origin of cancer in newborn twins. Nature Communications, October 6, 2026. doi.org

ScienceAlert, Scientists Trace How Cancer Passed Between Twins Before Birth, October 9, 2026. sciencealert.com

New Scientist, Rare cancer spread between twins in utero, October 14, 2026. newscientist.com

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