Obesity-associated changes in molecular biology of primary breast cancer.
Ha-Linh NguyenTatjana GeukensMarion MaetensSamuel A J R AparicioAyse BassezÅke BorgJane BrockAnnegien BroeksCarlos CaldasFatima CardosoMaxim De SchepperMauro DelorenziCaroline A DrukkerAnnuska M GlasAndrew R GreenEdoardo IsnaldiJórunn EyfjörðHazem KhoutStian KnappskogSavitri KrishnamurthySunil R LakhaniAnita LangerodJohn W M MartensAmy E McCart ReedLeigh MurphyStefan NaulaertsSerena Nik-ZainalInes NevelsteenPatrick NevenMartine J PiccartCoralie PoncetKevin PunieColin PurdieEmad A RakhaAndrea RichardsonEmiel RutgersAnne-Vincent SalomonPeter Thomas SimpsonMarjanka K SchmidtChristos SotiriouPaul N SpanKiat Tee Benita TanAlastair ThompsonStefania TommasiKaren Van BaelenMarc Van de VijverSteven Van LaereLaura van 't VeerGiuseppe VialeAlain ViariHanne VosAnke T WitteveenHans P M W WildiersGiuseppe FlorisAbhishek Dinkarnath GargAnn SmeetsDiether LambrechtsElia Mario BiganzoliFrançois RichardChristine DesmedtPublished in: Nature communications (2023)
Obesity is associated with an increased risk of developing breast cancer (BC) and worse prognosis in BC patients, yet its impact on BC biology remains understudied in humans. This study investigates how the biology of untreated primary BC differs according to patients' body mass index (BMI) using data from >2,000 patients. We identify several genomic alterations that are differentially prevalent in overweight or obese patients compared to lean patients. We report evidence supporting an ageing accelerating effect of obesity at the genetic level. We show that BMI-associated differences in bulk transcriptomic profile are subtle, while single cell profiling allows detection of more pronounced changes in different cell compartments. These analyses further reveal an elevated and unresolved inflammation of the BC tumor microenvironment associated with obesity, with distinct characteristics contingent on the estrogen receptor status. Collectively, our analyses imply that obesity is associated with an inflammaging-like phenotype. We conclude that patient adiposity may play a significant role in the heterogeneity of BC and should be considered for BC treatment tailoring.
Keyphrases
- single cell
- end stage renal disease
- body mass index
- weight gain
- insulin resistance
- ejection fraction
- weight loss
- metabolic syndrome
- type diabetes
- chronic kidney disease
- newly diagnosed
- prognostic factors
- bariatric surgery
- stem cells
- estrogen receptor
- adipose tissue
- machine learning
- physical activity
- genome wide
- high fat diet induced
- bone marrow
- young adults
- data analysis