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Author Spotlight: Exploring the Role of FAM83A in Cervical Cancer
Published on: February 9, 2024
Prospects of molecularly-targeted therapies for cervical cancer treatment
Antonio Carlos de Freitas, Maria da Conceição Gomes Leitão, Eliane Campos Coimbra1
1Laboratory of Molecular Studies and Experimental Therapy Studies, Department of Genetics, Federal University of Pernambuco, Cidade Universitária, CEP 50.670-901, Recife - Pernambuco, Brazil. acf_ufpe@yahoo.com.br.
Abstract:
Cervical cancer is the third most common cancer among women worldwide and is responsible for 275.000 deaths each year. The development of cervical cancer has been linked to cell cycle disturbances caused by persistent expression of high- risk HPV oncoproteins (E5, E6 and E7), which modulate the expression of host genes and cellular microRNAs. An estimated 5 million women throughout the world are currently infected by HPV and several of them will develop invasive cervical cancer. Despite failures in conventional screening tests, approved therapies have no direct effect on HPV infection. In view of this, effective therapy for cervical cancer is still urgently needed, particularly in developing countries where more than 85% of fatal cases occur. In this paper we review the current molecular targeted therapies which are being explored and may have a significant impact on the treatment of HPV- related cervical dysplasia and carcinoma.
Insights
Cervical cancer, a leading cause of death for women globally, is linked to persistent high-risk human papillomavirus (HPV) infections. This review explores molecular targeted therapies for HPV-related cervical dysplasia and carcinoma, addressing an urgent need for effective treatments.
Area of Science:
- Oncology
- Virology
- Molecular Biology
Background:
- Cervical cancer is a major global health concern, particularly in developing nations, causing significant mortality.
- Persistent high-risk human papillomavirus (HPV) oncoproteins (E5, E6, E7) disrupt the cell cycle and gene expression, contributing to cervical cancer development.
- Current therapies are insufficient, as they do not directly target HPV infection, highlighting the need for novel treatment strategies.
Purpose of the Study:
- To review current molecular targeted therapies for HPV-related cervical dysplasia and carcinoma.
- To highlight potential therapeutic strategies that may impact the treatment of cervical cancer.
- To address the urgent need for effective cervical cancer treatments, especially in resource-limited settings.
Main Methods:
- Literature review of molecular targeted therapies for cervical cancer.
- Analysis of the role of HPV oncoproteins in cervical carcinogenesis.
- Examination of emerging therapeutic approaches targeting HPV-related pathways.
Main Results:
- The review identifies several molecular targeted therapies under investigation for cervical cancer.
- These therapies aim to counteract the effects of HPV oncoproteins and restore normal cellular function.
- The potential impact of these therapies on treating cervical dysplasia and carcinoma is discussed.
Conclusions:
- Molecular targeted therapies show promise for the treatment of HPV-related cervical cancer.
- Further research and clinical trials are necessary to validate these approaches.
- Effective treatments are crucial, particularly for high-burden regions globally.
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