Abolaji Olagunju

Mr. Abolaji Olagunju

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 July 2020 in International Journal of Travel Medicine and Global Health
Verified
Journal Article
Open access
PDF file
AOAbolaji Olagunju
Abolaji Olagunju
IOIfeoluwa Peace Oladapo
Ifeoluwa Peace Oladapo
SKSamson Oluwapelumi Kosemani
Samson Oluwapelumi Kosemani
FOFolashade Gloria Olorunfemi
Folashade Gloria Olorunfemi
AAAdesewa Sukurat Adeyemo
Adesewa Sukurat Adeyemo
With the occurrence of a mysterious pneumonia in the Hubei province (Wuhan) of China in December 2019, a different coronavirus, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has commanded global awareness and has been named by the World Health Organization (WHO) as a public health emergency of international concern. Two other coronavirus infections (SARS and MERS) were also characterized by severe respiratory distress in 2002-2003. In addition to the new coronavirus, the emerging infectious diseases resulting in universal spread are caused by the β-coronavirus strains. Even though coronaviruses typically target the upper and/or lower respiratory tract, viral shedding into the plasma or serum is frequent, and the human coronavirus (CoV) represents 15%–30% of respiratory syndromes, including common colds. Based on a recent hypothesis, SARS-CoV-2 has been shown to induce lung injury by inhibiting the angiotensin converting enzyme-2 (ACE-2) and could possibly attack organs with high expression. With the lack of a vaccine or major treatment for the disease, palliative care is provided for individuals already infected with the virus. The aim of this review is to discuss the influence and relationship of the coronavirus, particularly SARS-CoV-2, on the respiratory system with a proposed mechanism of action in lung injury and pathogenesis.

15 September 2025
Verified
Book Chapter
Open access
PDF file
John Oluwafemi TeiboJohn Oluwafemi Teibo
John Oluwafemi Teibo
FAFestus Adebayo Atiba
Festus Adebayo Atiba
AAAyomide Oluwadarasimi Adebesin
Ayomide Oluwadarasimi Adebesin
AOAbolaji Olagunju
Abolaji Olagunju
TTTitilade Kehinde Ayandeyi Teibo
Titilade Kehinde Ayandeyi Teibo
Gaber El-Saber BatihaGaber El-Saber Batiha
Gaber El-Saber Batiha
Cancer is one of the leading causes of death worldwide and a major global public health concern, especially in sub-Saharan Africa (SSA). Recent advances in the five pillars of cancer treatment: surgery, radiation, chemotherapy, targeted therapies, and immunotherapy have enhanced the treatment of cancers, with immunotherapy leading as a frontier in the treatment of cancers. However, in SSA, there are limitations to the application of this frontier treatment due to minimal or no representation of Africans in most clinical trials involving cancer immunotherapy. To achieve desired treatment successes in SSA, special attention needs to be paid to how these advances can be applied in SSA settings. In this chapter, we examine major barriers to the adoption of immunotherapy, such as high treatment costs, a lack of biomarker testing and genomic sequencing, underrepresentation in clinical trials, and insufficient healthcare infrastructure. We concluded with strategic proposals for overcoming these constraints, including greater funding for cancer research in SSA, extension of local clinical trials, capacity training, and policy reforms. Addressing these disparities is critical for ensuring equitable access to immunotherapy and improving cancer outcomes throughout SSA.

11 April 2026 in Current Oncology Reports
Verified
Journal Article
Open access
PDF file
AOAbolaji Olagunju
Abolaji Olagunju
ABAyoade Desmond Babalola
Ayoade Desmond Babalola
SNSarah Eseroghene Najophe
Sarah Eseroghene Najophe
OFOluwabukola Mary Farodoye
Oluwabukola Mary Farodoye
TOTitilayomi Ayomide Otenaike
Titilayomi Ayomide Otenaike
John Oluwafemi TeiboJohn Oluwafemi Teibo
John Oluwafemi Teibo
Purpose of Review: Genomic profiling has significantly advanced precision oncology; however, relying solely on genome-driven approaches is often insufficient to capture the full molecular complexity of cancer. Proteogenomics integrates proteomics, transcriptomics, and genomic analyses to provide a more holistic view of tumor biology by revealing how genetic alterations translate into functional consequences at the protein level. Recent Findings: This multidimensional framework enhances the ability to identify clinically actionable biomarkers, uncover dysregulated pathways, and understand tumor heterogeneity with greater precision. By advancing tumor molecular profiling, proteogenomics offers the potential to refine tumor classification, improve diagnostic accuracy, and better tailor therapeutic strategies to individual patient needs. This review examines the expanding role of proteogenomics as an essential tool in personalized cancer management. Key analytical platforms, including mass spectrometry–based proteomics and phosphoproteomics, next-generation sequencing, and integrative computational pipelines, are discussed. Summary: We also highlight illustrative applications across diverse malignancies, including melanoma and hepatocarcinoma (HCC), where proteogenomic insights have informed therapeutic decision-making, revealed novel drug targets, and improved understanding of treatment resistance mechanisms; challenges and future prospects were also discussed. These advancements collectively highlight the increasing significance of proteogenomics in the evolution of precision oncology and the centrality of integrated molecular profiling in personalized cancer treatment.