Transcript for High Yield: Cervical cancer
High Yield: Cervical cancer
At the gynecology clinic, 28-year-old Luciana comes in because she was told that her Pap smear showed abnormal cervical cells.
She is totally asymptomatic and her previous pap smear from 3 years ago was normal.
Next, there is 36-year-old Cassie who presents to the office after noticing vaginal bleeding after sexual intercourse.
There’s no associated pain with urinating, bloody urine, constipation or pelvic pain.
She admits she has never done a pap test in her life. Pelvic exam shows a friable mass growing on the cervix.
On further history, both have been sexually active with multiple sexual partners and use oral contraceptive pills as their method of contraception.
Both Luciana and Cassie have different types of cervical pathologies.
So, first let’s talk physiology real quick.
The cervical canal can be divided into two sections.
The endocervix is closer to the uterus, and is lined by columnar epithelial cells.
The ectocervix is continuous with the vagina and it’s lined by mature squamous epithelial cells.
Where the squamous epithelium of the ectocervix and the columnar epithelium of the endocervix meet, there’s a line called the squamocolumnar junction.
For your exams, it’s necessary to remember that, right where the two types of cells meet, there’s the transformation zone, which is where cells multiply and transform into immature squamous epithelium through a process called metaplasia.
Now, metaplasia is when a stimulus, usually a stressor, causes the stem cells in a region to differentiate into another type of cells that replaces the typical cell type in that region.
For example with Barrett’s esophagus, chronic stomach acid irritation causes the normal stratified squamous cells that line the esophagus to get replaced by simple columnar cells.
This is different from dysplasia where fully differentiated cells turn into immature cells that have varying shape and nuclear morphology.
Metaplasia is usually reversible if the stressor is removed while only mild or moderate dysplasia is reversible.
So, in the cervix, right at the basal layer of the transformation zone is where dysplasia might start.
This is also known as cervical intraepithelial neoplasia or squamous epithelial lesion.
In most cases, cervical intraepithelial neoplasia is linked to HPV infection, particularly high-risk strains, like HPV 16, 18, 31 and 33.
Don’t confuse these with low-risk strains, like HPV 6 and 11, which are responsible for warts.
HPV viruses are DNA viruses that invade stratified squamous epithelial cells.
They especially prefer immature squamous cells, so areas under constant friction or irritation with high cell turnover, like the vocal cords or the anus, is especially vulnerable.
In the cervix, the virus inserts itself into the immature squamous cells of the transformation zone and then integrates its DNA into the host DNA.
An important fact to know is what sets low- and high-risk HPV strains apart.
And that is the ability of the high-risk ones to make huge amounts of two proteins, E6 and E7, using the host DNA.
These proteins are responsible for pushing mature squamous cells through the cell replication cycle by blocking the action of tumor suppressor genes.
Specifically, remember that E6 inhibits p53, while E7 inhibits retinoblastoma tumor suppressor gene product, or pRB for short.
The end result is uncontrolled replication of cervical epithelial cells which are resistant to apoptosis, or normal programmed cell death.
Since HPV is a sexually transmitted infection, a high yield fact to remember is that the number one risk factor for it: is having multiple sexual partners and not using condoms.
Other factors also increase the risk, like early age at first sexual intercourse, smoking, immunosuppression, like in HIV infected individuals or transplant recipients, and low socioeconomic status.
Now, in cervical intraepithelial neoplasia, dysplastic, HPV-infected epithelial cells are often described as “koilocytes”.
These are immature squamous cells with dense irregularly staining cytoplasm and perinuclear clearing, resembling a halo.
And these cells pile up in the cervical epithelium, starting from the basal layer and moving upwards.
So, depending on how much of the epithelium is involved, thickness-wise, cervical epithelial neoplasia is divided into grades.
Grade 1 or CIN I affects the lower one-third of the epithelium, grade 2 or CIN II affects two-thirds, grade 3 or CIN III affects almost all of the epithelium, and finally carcinoma in situ or CIS affects the entire thickness of the epithelium.
Eventually, carcinoma in situ can progress to invasive cervical cancer, which is when cancerous cells break through the epithelial basement membrane and into the cervical stroma.
These are mostly squamous cell carcinomas.
The second most common type, also associated with HPV, is cervical adenocarcinoma, which involves the epithelial gland cells of the cervix.
But either way, what you need to remember is that CIN classically progresses in a stepwise fashion, meaning from CIN I to CIN II to CIN III to CIS and, eventually, to invasive carcinoma.
However, progression doesn’t always occur, especially in low grades.
In other words, the higher the grade, the more likely it is to progress to carcinoma and the less likely it is to regress to normal.
- "Robbins Basic Pathology"Elsevier(2017)
- "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)"McGraw-Hill Education / Medical(2018)
- "Human Papillomavirus (HPV), HPV-Related Disease, and the HPV Vaccine"Rev Obstet Gynecol(2008)
- "Cervical cancer"Am Fam Physician(2000)
- "Detection of human papillomavirus DNA in anal intraepithelial neoplasia and anal cancer"Cancer Res(1991)
- "Cervical intraepithelial neoplasia disease progression is associated with increased vaginal microbiome diversity"Scientific Reports(2015)
- "HPV type-related chromosomal profiles in high-grade cervical intraepithelial neoplasia"BMC Cancer(2012)