Decoding Cancer Evolution: Integrating Genetic and Non-Genetic Insights
نویسندگان
چکیده
The development of cancer begins with cells transitioning from their multicellular nature to a state akin unicellular organisms. This shift leads breakdown in the crucial regulators inherent multicellularity, resulting emergence diverse cell subpopulations that have enhanced adaptability. presence different within tumour, known as intratumoural heterogeneity (ITH), poses challenges for treatment. In this review, we delve into dynamics multicellularity unicellularity during onset and progression. We highlight role genetic non-genetic factors, well tumour microenvironment, promoting ITH evolution. Additionally, shed light on latest advancements omics technologies allow in-depth analysis tumours at single-cell level spatial organization tissue. Obtaining such detailed information is deepening our understanding evolutionary paths cancer, allowing effective therapies targeting key drivers
منابع مشابه
Genetic and Epigenetic of Medullary Thyroid Cancer
Medullary thyroid carcinoma (MTC) is an infrequent calcitonin-producing neuroendocrine tumor that initiates from the parafollicular C cells of the thyroid gland. Several genetic and epigenetic alterations are collaterally responsible for medullary thyroid carcinogenesis. In this review article, we shed light on all the genetic and epigenetic hallmarks of MTC. From the genetic perspective, RET, ...
متن کاملGenetic insights into breast cancer risk
Since the identification of BRCA1 and BRCA2 much has been learned about the role of mutations in these genes and how they relate to disease risk. The primary population that has been screened for mutations in these genes has been women who have a family history of early onset breast and or ovarian cancer. The tumour characteristics of women who harbour a BRCA1 mutation are similar to those iden...
متن کاملNew Insights on Genetic Features of Neu-Laxova Syndrome
ABSTRACTBackground: This study aimed to present a rare case of Neu-Laxova syndrome (NLS) and review the newly revealed genetic features of the disease in hopes to find a way for early interventions.Case report: Female newborn with NLS was born at 30 weeks of gestation to consanguineous parents. The last prenatal ultrasound imaging revealed severe intrauterine growth restriction and microcephaly...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Genes
سال: 2023
ISSN: ['2073-4425']
DOI: https://doi.org/10.3390/genes14101856