Question
A. | E6 & E7 |
B. |
E5 |
C. |
E1 |
D. |
E2 |
Correct Answer � A Explanation |
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Ans. A. E6 & E7
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Human papillomavirus (HPV) infection is the main risk factor for the development of several cancers, such as head and neck cancer and cervical cancer.
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Currently, the two major viral oncoproteins, E6 and E7, are considered targets for developing therapeutic vaccines because they drive cellular immortalization and maintain the transformed phenotype during tumor progression.
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They exert functions by binding with many cellular proteins to activate cancer hallmarks.
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For example, E6 and E7 can interact with the pro-apoptotic proteins p53 and retinoblastoma tumor suppressor protein (pRB), respectively, to promote the targeted degradation of proteins with different crucial roles in tumorigenesis.
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Moreover, the joint functioning of the E6 and E7 oncoproteins is required from early to later stages of HPV-induced malignancy.
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In addition, the sequences of both proteins are well-conserved across a broad range of HPV subtypes.
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Thus, the two oncoproteins are considered to be potential targets for therapeutic interventions using vaccines against HPV-associated tumors.
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Continued expression of the two HPV oncoproteins is required to maintain the malignant phenotype; however, both E6 and E7 can individually transform primary cells through interacting with different cellular targets, and their major roles in tumorigenesis are different.
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In cervical tissue, E7 appears to serve as the dominant oncogene to produce the early stages of reproductive tract carcinomas, whereas E6 promotes the later stage of tumor progression.
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Since the E6 and E7 oncoproteins are dominant at different stages during tumor development, targeting both the E6 and E7 oncoproteins would be a promising approach for the development of therapeutic vaccines that could provide comprehensive therapeutic effects in HPV-mediated cancers.