Metabolic reprogramming signature predicts prognosis and immune landscape in small cell lung cancer: MOCS2 validation and implications for personalized therapy
IntroductionSmall cell lung cancer (SCLC) remains a leading cause of cancer mortality worldwide, characterized by rapid progression and poor clinical outcomes, and the function of metabolic reprogramming remains unclear in SCLC.MethodsWe performed multi-omics analysis using public SCLC datasets, ana...
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Frontiers Media S.A.
2025-05-01
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| Series: | Frontiers in Molecular Biosciences |
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| Online Access: | https://www.frontiersin.org/articles/10.3389/fmolb.2025.1592888/full |
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| author | Junyan Wang Panpan Sun Fan Zhang Yu Xu Shenghu Guo |
| author_facet | Junyan Wang Panpan Sun Fan Zhang Yu Xu Shenghu Guo |
| author_sort | Junyan Wang |
| collection | DOAJ |
| description | IntroductionSmall cell lung cancer (SCLC) remains a leading cause of cancer mortality worldwide, characterized by rapid progression and poor clinical outcomes, and the function of metabolic reprogramming remains unclear in SCLC.MethodsWe performed multi-omics analysis using public SCLC datasets, analyzing single-cell RNA sequencing to identify metabolic reprogramming patterns between chemotherapy-resistant and sensitive samples. Bulk RNA sequencing from GSE60052 and cBioportal cohorts was used to identify metabolism-related gene modules through WGCNA and develop a Gradient Boosting Machine prognostic model. Functional validation of MOCS2, the top-ranked gene in our model, was conducted through siRNA knockdown experiments in SCLC cell lines.ResultsSingle-cell analysis revealed distinct metabolic reprogramming patterns between chemotherapy-resistant and sensitive samples. WGCNA identified a turquoise module strongly correlated with metabolic reprogramming (cor = 0.56, P < 0.005). The GBM-based prognostic model demonstrated excellent performance (C-index = 0.915) with MOCS2, USP39, SMYD2, GFPT1, and PRKRIR identified as the most important variables. Kaplan-Meier analysis confirmed significant survival differences between high-risk and low-risk groups in both validation cohorts (P < 0.001). In vitro experiments showed that MOCS2 knockdown significantly reduced SCLC cell proliferation, colony formation, and migration capabilities (all P < 0.01), confirming its crucial role in regulating SCLC cell biology. Immunological characterization revealed distinct immune landscapes between risk groups, and drug sensitivity analysis identified five compounds with significantly different response profiles between risk groups.ConclusionOur study established a robust metabolism-based prognostic model for SCLC that effectively stratifies patients into risk groups with distinct survival outcomes, immune profiles, and drug sensitivity patterns. Functional validation experiments confirmed MOCS2 as an important regulator of SCLC cell proliferation and migration, providing valuable insights for treatment selection and prognosis prediction in SCLC. |
| format | Article |
| id | doaj-art-98e4e9dfc7ab4e08ad7e30cc8fcb447c |
| institution | OA Journals |
| issn | 2296-889X |
| language | English |
| publishDate | 2025-05-01 |
| publisher | Frontiers Media S.A. |
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| series | Frontiers in Molecular Biosciences |
| spelling | doaj-art-98e4e9dfc7ab4e08ad7e30cc8fcb447c2025-08-20T02:31:00ZengFrontiers Media S.A.Frontiers in Molecular Biosciences2296-889X2025-05-011210.3389/fmolb.2025.15928881592888Metabolic reprogramming signature predicts prognosis and immune landscape in small cell lung cancer: MOCS2 validation and implications for personalized therapyJunyan Wang0Panpan Sun1Fan Zhang2Yu Xu3Shenghu Guo4Medical Oncology Department, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, ChinaDepartment of Psychiatry, Hebei Province Rong-Jun Hospital, Baoding, Hebei, ChinaMedical Oncology Department, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, ChinaMedical Oncology Department, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, ChinaDepartment of Immuno-Oncology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, ChinaIntroductionSmall cell lung cancer (SCLC) remains a leading cause of cancer mortality worldwide, characterized by rapid progression and poor clinical outcomes, and the function of metabolic reprogramming remains unclear in SCLC.MethodsWe performed multi-omics analysis using public SCLC datasets, analyzing single-cell RNA sequencing to identify metabolic reprogramming patterns between chemotherapy-resistant and sensitive samples. Bulk RNA sequencing from GSE60052 and cBioportal cohorts was used to identify metabolism-related gene modules through WGCNA and develop a Gradient Boosting Machine prognostic model. Functional validation of MOCS2, the top-ranked gene in our model, was conducted through siRNA knockdown experiments in SCLC cell lines.ResultsSingle-cell analysis revealed distinct metabolic reprogramming patterns between chemotherapy-resistant and sensitive samples. WGCNA identified a turquoise module strongly correlated with metabolic reprogramming (cor = 0.56, P < 0.005). The GBM-based prognostic model demonstrated excellent performance (C-index = 0.915) with MOCS2, USP39, SMYD2, GFPT1, and PRKRIR identified as the most important variables. Kaplan-Meier analysis confirmed significant survival differences between high-risk and low-risk groups in both validation cohorts (P < 0.001). In vitro experiments showed that MOCS2 knockdown significantly reduced SCLC cell proliferation, colony formation, and migration capabilities (all P < 0.01), confirming its crucial role in regulating SCLC cell biology. Immunological characterization revealed distinct immune landscapes between risk groups, and drug sensitivity analysis identified five compounds with significantly different response profiles between risk groups.ConclusionOur study established a robust metabolism-based prognostic model for SCLC that effectively stratifies patients into risk groups with distinct survival outcomes, immune profiles, and drug sensitivity patterns. Functional validation experiments confirmed MOCS2 as an important regulator of SCLC cell proliferation and migration, providing valuable insights for treatment selection and prognosis prediction in SCLC.https://www.frontiersin.org/articles/10.3389/fmolb.2025.1592888/fullmetabolic reprogrammingsmall cell lung cancerprognosisimmune microenvironmentdrug sensitivity |
| spellingShingle | Junyan Wang Panpan Sun Fan Zhang Yu Xu Shenghu Guo Metabolic reprogramming signature predicts prognosis and immune landscape in small cell lung cancer: MOCS2 validation and implications for personalized therapy Frontiers in Molecular Biosciences metabolic reprogramming small cell lung cancer prognosis immune microenvironment drug sensitivity |
| title | Metabolic reprogramming signature predicts prognosis and immune landscape in small cell lung cancer: MOCS2 validation and implications for personalized therapy |
| title_full | Metabolic reprogramming signature predicts prognosis and immune landscape in small cell lung cancer: MOCS2 validation and implications for personalized therapy |
| title_fullStr | Metabolic reprogramming signature predicts prognosis and immune landscape in small cell lung cancer: MOCS2 validation and implications for personalized therapy |
| title_full_unstemmed | Metabolic reprogramming signature predicts prognosis and immune landscape in small cell lung cancer: MOCS2 validation and implications for personalized therapy |
| title_short | Metabolic reprogramming signature predicts prognosis and immune landscape in small cell lung cancer: MOCS2 validation and implications for personalized therapy |
| title_sort | metabolic reprogramming signature predicts prognosis and immune landscape in small cell lung cancer mocs2 validation and implications for personalized therapy |
| topic | metabolic reprogramming small cell lung cancer prognosis immune microenvironment drug sensitivity |
| url | https://www.frontiersin.org/articles/10.3389/fmolb.2025.1592888/full |
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