Wilms' tumour: a systematic review of risk factors and meta-analysis

Anna Chu1, Julia E Heck, Karina Braga Ribeiro

  • 1Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.

Insights

Maternal pesticide exposure, high birthweight, and preterm birth are linked to an increased risk of Wilms' tumour in children. Later-born children showed a decreased risk, suggesting perinatal and environmental factors influence this childhood cancer.

Area of Science:

  • Pediatric Oncology
  • Environmental Epidemiology
  • Perinatal Health

Background:

  • Wilms' tumour is the most common pediatric renal cancer, affecting children under 15.
  • Understanding its etiology is crucial for prevention and early detection strategies.

Purpose of the Study:

  • To systematically review epidemiological studies on perinatal and environmental risk factors for Wilms' tumour.
  • To synthesize evidence on factors influencing the incidence of this childhood cancer.

Main Methods:

  • Conducted a comprehensive literature search across major databases (Medline, LILACS, Web of Science, Dissertation Abstracts).
  • Included 37 epidemiological studies (14 cohort, 21 case-control, 2 case-cohort) examining risk factors.
  • Prioritized studies with population-based controls and assessed potential publication bias.

Main Results:

  • Maternal pesticide exposure before birth, high birthweight, and preterm birth were significantly associated with increased Wilms' tumour risk (ORs ranging from 1.36 to 1.44).
  • Second or later birth order was associated with a significantly decreased risk (OR = 0.82).
  • Maternal hypertension showed a non-significant increased risk (OR = 1.30).

Conclusions:

  • Perinatal factors such as birthweight and gestational age, alongside environmental exposures like pesticides, play a role in Wilms' tumour development.
  • Birth order may also influence risk, with later-born children having a lower likelihood.
  • Further research is warranted to confirm findings and explore underlying mechanisms.

Related Concept Videos

The Retinoblastoma Gene01:20

The Retinoblastoma Gene

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
Canonical Wnt Signaling Pathway02:54

Canonical Wnt Signaling Pathway

The gene encoding the main signaling molecules of the Wnt signaling pathways (the Wnt proteins) was discovered almost four decades ago by Nüsslein-Volhard and Wieschaus. They identified and originally named the gene "wingless" (wg) after a phenotype discovered during their landmark genetic screen in Drosophila for body pattern defects. At around the same time, another researcher named Harold Varmus found that a murine tumor virus activates the mammalian wg homolog, Int-1, which results in tumor...
Non-Canonical Wnt Signaling Pathways01:41

Non-Canonical Wnt Signaling Pathways

Wnt is a zygotic effect gene that is expressed during very early embryonic development. It regulates various processes in animals starting from early development through the adult stage, such as organogenesis in the embryo and maintenance of neuronal and blood stem cells. Wnt proteins can induce a wide variety of intracellular pathways depending upon the specific abilities of different Wnt ligands to form a complex with shared and cognate receptors in the presence of different co-receptors. The...