## Abstract Human wart virus was isolated from plantar warts. After extraction of its DNA, component I was transcribed into radioactive complementary RNA (cRNA) with the aid of Escherichia coli RNA polymerase. The resulting cRNA annealed specifically to wart viral DNA and was used as a probe for th
Attempts to detect virus-specific DNA in human tumors. II. Nucleic acid hybridizations with complementary RNA of human herpes group viruses
✍ Scribed by Harald Zur Hausen; Heinrich Schulte-Holthausen; Hans Wolf; Kristina Dörries; Herwig Egger
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- French
- Weight
- 543 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
DNA derived from various human malignant and non‐malignant tissues was hybridized with radioactive complementary RNA (cRNA) synthetized in vitro with the aid of E.coli‐RNA‐polymerase by using DNA of human herpes group viruses as templates. Epstein‐Barr virus (EBV)‐specific cRNA annealed significantly with DNA from nasopharyngeal carcinoma biopsies as well as with DNA preparations from leukocytes, bone marrow, lymph node and spleen of some patients with infectious mononucleosis. No significant hybridization was observed with either herpes simplex type 2 or type 1 cRNA and DNA from ten cervical carcinoma biopsies. cRNA of human cytomegalovirus and varicellazoster virus did not hybridize with DNA from Kaposi's sarcoma or DNA from heavily infiltrated spleens of patients with Hodgkin's disease. These data do not exclude a role of these herpes viruses in the etiology of cervical carcinoma, Kaposi's sarcoma and Hodgkin's disease. They show, however, that such a relationship (if it exists) must differ quantitatively to a considerable extent from the one observed with EBV in EBV‐associated tumors.
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