Cancer cells arise from normal cells due to genetic mutations affecting cell division regulation.
They exhibit uncontrolled division, potentially invading other tissues and disrupting organ function.
Despite this, normal cell division is crucial for all life forms.
Cell division is fundamental for reproduction and the continuation of life; cells come from preexisting cells.
Asexual Reproduction: Offspring are genetic copies of the parent, resulting in identical progeny.
Sexual Reproduction: Produces offspring with genetic diversity.
Prokaryotes reproduce asexually via binary fission, meaning they divide in half.
A single circular DNA molecule replicates, copies move apart, and the cell divides.
Eukaryotic cells contain more genes organized into multiple chromosomes within a nucleus.
Chromosomes become visible only during cell division and duplicate to form sister chromatids connected at a centromere.
The cell cycle is a sequence of events from cell formation to division.
Consists primarily of Interphase (G1, S, G2) and the M phase (mitosis).
Mitosis ensures equal distribution of chromosomes into two daughter nuclei, with key processes including the formation of a mitotic spindle.
Sister chromatids are separated to opposite poles forming two new nuclei.
Cytokinesis varies in plant and animal cells:
Animal cells: form a cleavage furrow.
Plant cells: form a cell plate.
Environmental factors can influence cell division; for example, cells typically only divide when attached to a surface.
Growth factors play a key role in regulating the cell cycle at checkpoints.
Cancer cells proliferate uncontrollably forming tumors, and malignant tumors can invade surrounding tissues.
Treatments such as radiation and chemotherapy target and disrupt cell division.
Somatic (body) cells contain homologous pairs of chromosomes; humans have 46 chromosomes (23 pairs).
Gametes (eggs and sperm) are haploid, containing a single chromosome set.
Sexual reproduction alternates between haploid and diploid stages.
Meiosis involves two divisions, producing four genetically unique haploid cells.
Crossing over occurs during meiosis I, enhancing genetic variation between sister chromatids.
Mitosis creates two identical diploid cells; meiosis yields four unique haploid cells.
Independent assortment during meiosis and random fertilization contribute to genetic diversity among offspring.
Crossing over during prophase I of meiosis increases genetic variability among gametes.
Nondisjunction (failure of chromosomes to separate properly) can lead to abnormal chromosome counts, causing disorders like Down syndrome (Trisomy 21).
A karyotype provides a visual inventory of chromosomes, useful for identifying chromosomal abnormalities.
Abnormalities in sex chromosomes may or may not affect survival, with some conditions like Klinefelter syndrome requiring medical attention.
Errors in cell division can lead to the emergence of new species, particularly through polyploidy.
Rearrangements in chromosome structure can cause genetic disorders or cancer due to deletions, duplications, inversions, or translocations.