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  2. Transcriptomic analysis reveals Streptococcus agalactiae activation of oncogenic pathways in cervical adenocarcinoma

Transcriptomic analysis reveals Streptococcus agalactiae activation of oncogenic pathways in cervical adenocarcinoma

  • Oncol Lett. 2024 Oct 3;28(6):588. doi: 10.3892/ol.2024.14720.
Hong Duc Thi Nguyen 1 Tan Minh Le 1 Da-Ryung Jung 2 Youngjae Jo 2 Yeseul Choi 1 Donghyeon Lee 1 Olive Em Lee 1 Junghwan Cho 3 Nora Jee-Young Park 3 4 5 Incheol Seo 6 Gun Oh Chong 3 7 8 Jae-Ho Shin 2 9 10 Hyung Soo Han 1 3 11
Affiliations

Affiliations

  • 1 Department of Biomedical Science, Graduate School, Kyungpook National University, Daegu 41944, Republic of Korea.
  • 2 Department of Applied Biosciences, Kyungpook National University, Daegu 41566, Republic of Korea.
  • 3 Clinical Omics Institute, Kyungpook National University, Daegu 41405, Republic of Korea.
  • 4 Department of Pathology, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea.
  • 5 Department of Pathology, Kyungpook National University Chilgok Hospital, Daegu 41404, Republic of Korea.
  • 6 Department of Immunology, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea.
  • 7 Department of Obstetrics and Gynecology, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea.
  • 8 Department of Obstetrics and Gynecology, Kyungpook National University Chilgok Hospital, Daegu 41404, Republic of Korea.
  • 9 Department of Integrative Biotechnology, Kyungpook National University, Daegu 41566, Republic of Korea.
  • 10 Next Generation Sequencing Core Facility, Kyungpook National University, Daegu 41566, Republic of Korea.
  • 11 Department of Physiology, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea.
Abstract

Cervical adenocarcinoma (AC), a subtype of uterine cervical Cancer (CC), poses a challenge due to its resistance to therapy and poor prognosis compared with squamous cervical carcinoma. Streptococcus agalactiae [group B Streptococcus (GBS)], a Gram-positive coccus, has been associated with cervical intraepithelial neoplasia in CC. However, the underlying mechanism interaction between GBS and CC, particularly AC, remains elusive. Leveraging The Cancer Genome Atlas public data and time-series transcriptomic data, the present study investigated the interaction between GBS and AC, revealing activation of two pivotal pathways: 'MAPK signaling pathway' and 'mTORC1 signaling'. Western blotting, reverse transcription-quantitative PCR and cell viability assays were performed to validate the activation of these pathways and their role in promoting Cancer cell proliferation. Subsequently, the present study evaluated the efficacy of two Anticancer drugs targeting these pathways (binimetinib and ridaforolimus) in AC cell treatment. Binimetinib demonstrated a cytostatic effect, while ridaforolimus had a modest impact on HeLa cells after 48 h of treatment, as observed in both cell viability and cytotoxicity assays. The combination of binimetinib and ridaforolimus resulted in a significantly greater cytotoxic effect compared to binimetinib or ridaforolimus monotherapy, although the synergy score indicated an additive effect. In general, the MAPK and mTORC1 signaling pathways were identified as the main pathways associated with GBS and AC cells. The combination of binimetinib and ridaforolimus could be a potential AC treatment.

Keywords

Streptococcus agalactiae; cervical adenocarcinoma; drug repurposing; signaling pathway; transcriptomic time-series analysis.

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