What factor(s) place a person at risk for developing cancer? (Select all that apply)
Smoking
Obesity
Tanning without sunscreen
Human papillomavirus (HPV)
Family history of cancer
Correct Answer : C,D,E
Choice A reason: Smoking introduces carcinogens like polycyclic aromatic hydrocarbons, damaging DNA and promoting mutations in lung, throat, and other tissues. Chronic exposure increases cancer risk, particularly lung cancer, by disrupting cellular repair mechanisms, making this a correct risk factor.
Choice B reason: Obesity increases cancer risk through chronic inflammation and hormonal imbalances, like elevated estrogen, linked to breast and endometrial cancers. However, it is not listed in the provided options, so it cannot be selected, though it is scientifically relevant.
Choice C reason: Tanning without sunscreen exposes skin to UV radiation, causing DNA damage in melanocytes and increasing melanoma risk. UV-induced mutations disrupt cell cycle regulation, promoting uncontrolled cell growth, making this a correct cancer risk factor.
Choice D reason: Human papillomavirus (HPV) causes cancers like cervical and oropharyngeal by integrating viral DNA into host cells, disrupting tumor suppressor genes. Chronic infection leads to cellular transformation, making this a correct risk factor for specific cancers.
Choice E reason: Family history of cancer indicates genetic predispositions, such as BRCA mutations, increasing risks for breast, ovarian, or other cancers. Inherited mutations impair DNA repair or cell cycle control, making this a correct risk factor for cancer development.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is C
Explanation
Choice A reason: Autosomal dominant disorders affect both genders equally, as they are not sex-linked. Heterozygous individuals express the disorder, not just males, due to the dominant allele on an autosome. The idea of females being carriers only applies to X-linked recessive disorders, making this choice scientifically inaccurate.
Choice B reason: Autosomal dominant disorders are caused by mutations on autosomes, not the Y chromosome, which is sex-linked and primarily affects males. These disorders do not typically skip generations, as the dominant allele is expressed in every affected individual, making this choice incorrect.
Choice C reason: In autosomal dominant disorders, a single mutated allele is sufficient for expression. An affected parent (heterozygous) has one normal and one mutated allele, leading to a 50% chance of passing the mutated allele to each child, causing the disorder. This genetic inheritance pattern makes this the correct choice.
Choice D reason: In autosomal dominant disorders, there is no "carrier" state as in recessive disorders, because heterozygous individuals express the disorder. The 50% probability applies to inheriting the disorder itself, not a carrier genotype, which is a concept relevant to autosomal recessive disorders, making this choice incorrect.
Correct Answer is A
Explanation
Choice A reason: Landing on the feet from a high fall causes axial loading, compressing the spinal column, often resulting in a compression injury to the spinal cord. This damages cord tissue, making this the correct choice.
Choice B reason: Transection involves complete severing of the spinal cord, typically from penetrating trauma. A fall causing compression is less likely to fully transect the cord, making this choice incorrect.
Choice C reason: Hyperflexion injuries occur when the spine bends forward excessively, as in whiplash. A fall on the feet causes vertical compression, not forward bending, making this choice incorrect for the injury.
Choice D reason: Hyperextension involves backward bending of the spine, not typical in a fall on the feet, which causes axial compression. This mechanism does not fit the described injury, making this choice incorrect.
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