Cancer does not typically follow a Mendelian pattern of inheritance because it is usually caused by
Specific combinations of alleles and environmental factors.
Correct! Sporadic cancer is caused by susceptibility gene variants and environmental exposures (exposure to chemicals, radiation), hormonal factors (levels of different hormones in the body), dietary habits, and other health behaviors.
Two gene variants, one dominant and one recessive and not environmental input.
Incorrect
Specific combinations of an environmental factor and one dominant gene variant.
Incorrect
Genes that cause death before birth.
Incorrect
All cancers reflect, at the most general level a defect in
DNA replication
Incorrect
Formation of mitochondria
Incorrect
The cell cycle
Correct! Uncontrolled cell proliferation is one of the main hallmarks of cancer, and tumor cells have acquired damage to genes that are directly involved in regulating the cell cycle. Damage is caused by mutations producing an oncogene with a dominant gain of function, and/or by mutations in tumor suppressor genes causing a recessive loss of function. Regardless of the genetic damage or type of cancer, the common feature is a disrupted cell cycle.
Cell membrane structure
Correct! A haploid sperm ferlitizing a diploid egg can result in an extra set of chromosomes because the egg is not haploid.
Sporadic cancers result from
Recessive or dominant germline mutation
Incorrect
Mutation in a sperm or oocyte
Incorrect
Exposure to a cancer-causing virus
Incorrect.
Recessive or dominant mutation in a somatic cell
Correct! Most cancers are caused by an accumulation of acquired mutations in somatic cells that happen mostly by chance and are not inherited. They are acquired sometime during a person’s lifetime. Sometimes these mutations are errors that occur during mitotic cell division. They can also be caused by things that damage a cell’s DNA, such as smoking, exposure to certain chemicals and radiation. The risk of sporadic mutations increases with age.
Matthew has the inherited form of retinoblastoma (RB). His disease is caused by
A germinal mutation in one RB allele and no mutation in the other allele
Incorrect
A germinal mutation in one RB allele and a somatic mutation in the other allele
Correct! In the inherited form of retinoblastoma, mutations in the RB1 gene appear to be inherited in an autosomal dominant pattern. Autosomal dominant inheritance suggests that one copy of the altered gene in each cell is sufficient to increase cancer risk. A person with inherited retinoblastoma may inherit an altered copy of the gene (a germinal mutation) from one parent, or the altered gene may be the result of a de novo mutation that occurs in an oocyte or sperm cell or just after fertilization. For retinoblastoma to develop, a somatic mutation in the involving the other copy of the RB1 gene must occur in retinal cells during the person's lifetime. This second mutation usually occurs in childhood, typically leading to the development of retinoblastoma in both eyes.
A somatic mutation in each copy of the RB gene in the same cell.
Incorrect
A somatic mutation in one of the RB genes in the same area of the retina of one eye
Incorrect