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Induction of uterine cancer with inactivated herpes simplex virus, types 1 and 2
Abstract:
A series of studies were performed to evaluate the oncogenic potential of inactivated herpes simplex viruses types 1 (HSV-1) and 2 (HSV-2) in the mouse cervix. HSV-1 or HSV-2 prepared in HEp-2 cell cultures and inactivated by exposure to formalin or ultraviolet light was applied to the mouse cervix for periods ranging from 20 to 90 weeks. Control mice were exposed for the same period to control fluids. Vaginal cytologic preparations from all animals were examined weekly to detect epithelial abnormalities. Animals were sacrificed and histopathological studies were carried out when cellular changes seen on vaginal smears resembled those indicative of premalignant or malignant changes as previously established in a similar model system using coal tar hydrocarbons. Other animals were exposed for periods up to 90 weeks, or until there was cellular evidence of invasive cancer. Cytologic and histologic materials were coded and evaluated without knowledge of whether they were from virus-exposed or control animals. Premalignant and malignant cervical lesions similar to those that occur in women were encountered in 78 to 90% of the virus-exposed animals. All controls were normal. Invasive cancer was detected in 24 to 60% of the animals and dysplasia was found in 18 to 66%. The yield of invasive cancer was twice as great after exposure to ultraviolet-inactivated HSV-2 as compared with formalin-inactivated virus. Various histologic grades of carcinoma of the cervix and endometrium were found. No primary lesions were found in the vagina or ovaries.
Insights
Inactivated herpes simplex viruses types 1 and 2 (HSV-1, HSV-2) induced cervical cancer in mice. Ultraviolet-inactivated HSV-2 was more potent than formalin-inactivated virus in causing invasive cervical cancer.
Area of Science:
- Oncology
- Virology
- Pathology
Background:
- Herpes simplex viruses (HSV-1, HSV-2) are common human pathogens.
- The oncogenic potential of inactivated HSV-1 and HSV-2 in cervical cancer models requires further investigation.
Purpose of the Study:
- To evaluate the oncogenic potential of inactivated herpes simplex viruses types 1 and 2 (HSV-1, HSV-2) in the mouse cervix.
- To compare the efficacy of formalin-inactivated versus ultraviolet-inactivated HSV in inducing cervical lesions.
Main Methods:
- Mice cervices were exposed to inactivated HSV-1 or HSV-2 for 20-90 weeks.
- Vaginal cytology and histopathology were used to detect epithelial abnormalities, premalignant, and malignant changes.
- Control groups received control fluids, and all evaluations were performed blinded.
Main Results:
- Premalignant and malignant cervical lesions developed in 78-90% of virus-exposed mice; controls remained normal.
- Invasive cervical cancer was detected in 24-60% of mice, with ultraviolet-inactivated HSV-2 yielding twice the cancer rate compared to formalin-inactivated virus.
- Various grades of cervical and endometrial carcinoma were observed, with no primary lesions in the vagina or ovaries.
Conclusions:
- Inactivated herpes simplex viruses can induce premalignant and malignant cervical lesions in mice.
- Ultraviolet inactivation of HSV-2 appears to enhance its oncogenic potential in the mouse cervix compared to formalin inactivation.
- This study establishes a mouse model for investigating HSV-associated cervical carcinogenesis.