# Uncovering Novel Anti-Lung Cancer Compounds: Insights from Marine Sponge-Derived Agents: A Bibliometric Review

**Authors:** Afshin Zare, Alireza Afshar, Nadiar M. Mussin, Asset A. Kaliyev, Raisa A. Aringazina, Nader Tanideh, Mahdi Mahdipour, Farhad Rahmanifar, Zhanna Zhussupova, Beibyt Tlektesuly Baizakov, Amin Tamadon

PMC · DOI: 10.30476/ijms.2024.103270.3646 · 2025-05-01

## TL;DR

This study explores marine sponge-derived compounds as potential new treatments for lung cancer, identifying promising candidates through bibliometric analysis and molecular docking.

## Contribution

The study identifies specific marine sponge compounds with strong binding to apoptotic receptors in lung cancer cells, offering new drug development opportunities.

## Key findings

- Alkaloids, sesquiterpenes, and quinones from marine sponges are highlighted as key anti-lung cancer compounds.
- Dactyloquinone B-D, dysidavarone D, smenohamien F, and sollasin E showed strong binding to apoptotic receptors in lung cancer cells.
- Pharmacological analyses suggest these compounds have promising effects and potential for further drug development.

## Abstract

Lung cancer remains a leading cause of cancer-related mortality, necessitating improved treatment strategies. This study collectively highlights the valuable potential of marine sponges as a source for discovering new anti-tumor agents.

We conducted a bibliometric analysis to identify anticancer compounds from marine sponges using PubMed (2018–2023). The search included keywords such as “marine sponge,” “cancer,” “neoplasm,” “proliferation,” “cytotoxicity,” “tumor,” “sesquiterpene,” “alkaloid,” and “quinones.” Inclusion criteria focused on studies related to lung cancer and marine sponge-derived compounds, excluding non-cytotoxic activities and unrelated species. Data were extracted in comma-separated values (CSV) format and analyzed via VOSviewer. Molecular docking identified compounds with strong binding to apoptotic receptors in lung cancer cells. PROTOX and Way2Drug tools predicted the pharmacological properties of selected compounds as potential drugs.

The bibliometric analysis identified alkaloids, sesquiterpenes, and quinones as key keywords. Dactyloquinone B-D, dysidavarone D, smenohamien F, and sollasin E demonstrated strong binding to apoptotic receptors in lung cancer cells, suggesting potential as anti-lung cancer drugs. Pharmacological analyses revealed promising effects and potential side effects, highlighting their suitability for further drug development. These findings provide a foundation for novel targeted therapies for lung cancer.

This study highlights the potential of alkaloids and sesquiterpenes derived from marine sponges as promising anti-lung cancer agents, emphasizing the need for further in vitro, in vivo, and clinical investigations to validate their therapeutic efficacy.

## Linked entities

- **Chemicals:** sollasin E (PubChem CID 9970696), sesquiterpenes (PubChem CID 139087999)
- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Diseases:** cytotoxic (MESH:D064420), Lung Cancer (MESH:D008175), cancer (MESH:D009369)
- **Chemicals:** quinones (MESH:D011809), alkaloid (MESH:D000470), Dactyloquinone B-D (-), sesquiterpene (MESH:D012717)

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12104544/full.md

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Source: https://tomesphere.com/paper/PMC12104544