Integration of single-cell RNA and bulk RNA sequencing revealed malignant ductal cell heterogeneity and prognosis signatures in pancreatic cancer
IntroductionPancreatic cancer is a highly malignant tumor of the digestive system with a dismal prognosis. Despite advances in diagnosis and treatment, overall survival remains extremely low. Early diagnostic markers and an improved understanding of tumor-microenvironment interactions are essential...
Saved in:
| Main Authors: | , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2025-07-01
|
| Series: | Frontiers in Immunology |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2025.1579184/full |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| _version_ | 1849429227460362240 |
|---|---|
| author | Haiyang Du Haiyang Du Gao Si Jiqing Si Xuejie Song Xuejie Song Fuchun Si Fuchun Si |
| author_facet | Haiyang Du Haiyang Du Gao Si Jiqing Si Xuejie Song Xuejie Song Fuchun Si Fuchun Si |
| author_sort | Haiyang Du |
| collection | DOAJ |
| description | IntroductionPancreatic cancer is a highly malignant tumor of the digestive system with a dismal prognosis. Despite advances in diagnosis and treatment, overall survival remains extremely low. Early diagnostic markers and an improved understanding of tumor-microenvironment interactions are essential for developing more effective therapies.MethodsWe analyzed 74 single-cell RNA sequencing (scRNA-seq) samples, performing unsupervised clustering and marker-gene expression profiling to define major cell types. Large-scale chromosomal copy-number variation (CNV) analysis distinguished malignant from non-malignant ductal cells. Non-negative matrix factorization (NMF) identified stage-associated gene modules, which were integrated with TCGA bulk-RNA data and machine-learning feature selection to pinpoint candidate prognostic genes. Two independent cohorts were used for validation. Regulatory network inference (pySCENIC) and ligand–receptor interaction analysis (CellPhoneDB) explored cross-talk between malignant cells and macrophages. Finally, in vitro knockdown of CTSV assessed its functional role in pancreatic cancer (PAC) cell proliferation and migration.ResultsThree prognosis-related genes—ANLN, NT5E, and CTSV—were selected based on their strong association with clinical stage and validated in external datasets. High expression of these genes correlated with poorer overall survival and an increased infiltration of M0 macrophages. CellPhoneDB predicted significant interactions between high-expression malignant ductal cells and M0 macrophages via CXCL14–CXCR4 and IL1RAP–PTPRF axes, with SPI1 identified as an upstream regulator of IL1RAP. In vitro CTSV knockdown significantly inhibited PAC cell proliferation and migration.DiscussionOur integrative single-cell and bulk-RNA workflow identifies ANLN, NT5E, and CTSV as novel prognostic biomarkers in pancreatic cancer and highlights a pro-tumorigenic interaction between malignant ductal cells and macrophages. Targeting CTSV or disrupting CXCL14–CXCR4 and IL1RAP–PTPRF signaling may offer new therapeutic avenues for PAC. |
| format | Article |
| id | doaj-art-aa1bbfefb3b1456ca87f8a60342303e3 |
| institution | Kabale University |
| issn | 1664-3224 |
| language | English |
| publishDate | 2025-07-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Immunology |
| spelling | doaj-art-aa1bbfefb3b1456ca87f8a60342303e32025-08-20T03:28:25ZengFrontiers Media S.A.Frontiers in Immunology1664-32242025-07-011610.3389/fimmu.2025.15791841579184Integration of single-cell RNA and bulk RNA sequencing revealed malignant ductal cell heterogeneity and prognosis signatures in pancreatic cancerHaiyang Du0Haiyang Du1Gao Si2Jiqing Si3Xuejie Song4Xuejie Song5Fuchun Si6Fuchun Si7Henan University of Chinese Medicine, Traditional Chinese Medicine (Zhongjing) School, Zhengzhou, ChinaHenan University of Chinese Medicine, Henan Key Laboratory of Traditional Chinese Medicine (TCM) Syndrome and Prescription Signaling, Henan International Joint Laboratory of Traditional Chinese Medicine (TCM) Syndrome and Prescription Signaling, Academy of Chinese Medical Sciences, Zhengzhou, ChinaDepartment of Orthopedic, The Third Hospital of Peking University, Beijing, ChinaHenan Hospital of Traditional Chinese Medicine (TCM), The Second Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou, ChinaHenan University of Chinese Medicine, Traditional Chinese Medicine (Zhongjing) School, Zhengzhou, ChinaHenan University of Chinese Medicine, Henan Key Laboratory of Traditional Chinese Medicine (TCM) Syndrome and Prescription Signaling, Henan International Joint Laboratory of Traditional Chinese Medicine (TCM) Syndrome and Prescription Signaling, Academy of Chinese Medical Sciences, Zhengzhou, ChinaHenan University of Chinese Medicine, Traditional Chinese Medicine (Zhongjing) School, Zhengzhou, ChinaHenan University of Chinese Medicine, Henan Key Laboratory of Traditional Chinese Medicine (TCM) Syndrome and Prescription Signaling, Henan International Joint Laboratory of Traditional Chinese Medicine (TCM) Syndrome and Prescription Signaling, Academy of Chinese Medical Sciences, Zhengzhou, ChinaIntroductionPancreatic cancer is a highly malignant tumor of the digestive system with a dismal prognosis. Despite advances in diagnosis and treatment, overall survival remains extremely low. Early diagnostic markers and an improved understanding of tumor-microenvironment interactions are essential for developing more effective therapies.MethodsWe analyzed 74 single-cell RNA sequencing (scRNA-seq) samples, performing unsupervised clustering and marker-gene expression profiling to define major cell types. Large-scale chromosomal copy-number variation (CNV) analysis distinguished malignant from non-malignant ductal cells. Non-negative matrix factorization (NMF) identified stage-associated gene modules, which were integrated with TCGA bulk-RNA data and machine-learning feature selection to pinpoint candidate prognostic genes. Two independent cohorts were used for validation. Regulatory network inference (pySCENIC) and ligand–receptor interaction analysis (CellPhoneDB) explored cross-talk between malignant cells and macrophages. Finally, in vitro knockdown of CTSV assessed its functional role in pancreatic cancer (PAC) cell proliferation and migration.ResultsThree prognosis-related genes—ANLN, NT5E, and CTSV—were selected based on their strong association with clinical stage and validated in external datasets. High expression of these genes correlated with poorer overall survival and an increased infiltration of M0 macrophages. CellPhoneDB predicted significant interactions between high-expression malignant ductal cells and M0 macrophages via CXCL14–CXCR4 and IL1RAP–PTPRF axes, with SPI1 identified as an upstream regulator of IL1RAP. In vitro CTSV knockdown significantly inhibited PAC cell proliferation and migration.DiscussionOur integrative single-cell and bulk-RNA workflow identifies ANLN, NT5E, and CTSV as novel prognostic biomarkers in pancreatic cancer and highlights a pro-tumorigenic interaction between malignant ductal cells and macrophages. Targeting CTSV or disrupting CXCL14–CXCR4 and IL1RAP–PTPRF signaling may offer new therapeutic avenues for PAC.https://www.frontiersin.org/articles/10.3389/fimmu.2025.1579184/fullpancreatic cancertumor microenvironmentCTSVmacrophagesCXCL14-CXCR4 |
| spellingShingle | Haiyang Du Haiyang Du Gao Si Jiqing Si Xuejie Song Xuejie Song Fuchun Si Fuchun Si Integration of single-cell RNA and bulk RNA sequencing revealed malignant ductal cell heterogeneity and prognosis signatures in pancreatic cancer Frontiers in Immunology pancreatic cancer tumor microenvironment CTSV macrophages CXCL14-CXCR4 |
| title | Integration of single-cell RNA and bulk RNA sequencing revealed malignant ductal cell heterogeneity and prognosis signatures in pancreatic cancer |
| title_full | Integration of single-cell RNA and bulk RNA sequencing revealed malignant ductal cell heterogeneity and prognosis signatures in pancreatic cancer |
| title_fullStr | Integration of single-cell RNA and bulk RNA sequencing revealed malignant ductal cell heterogeneity and prognosis signatures in pancreatic cancer |
| title_full_unstemmed | Integration of single-cell RNA and bulk RNA sequencing revealed malignant ductal cell heterogeneity and prognosis signatures in pancreatic cancer |
| title_short | Integration of single-cell RNA and bulk RNA sequencing revealed malignant ductal cell heterogeneity and prognosis signatures in pancreatic cancer |
| title_sort | integration of single cell rna and bulk rna sequencing revealed malignant ductal cell heterogeneity and prognosis signatures in pancreatic cancer |
| topic | pancreatic cancer tumor microenvironment CTSV macrophages CXCL14-CXCR4 |
| url | https://www.frontiersin.org/articles/10.3389/fimmu.2025.1579184/full |
| work_keys_str_mv | AT haiyangdu integrationofsinglecellrnaandbulkrnasequencingrevealedmalignantductalcellheterogeneityandprognosissignaturesinpancreaticcancer AT haiyangdu integrationofsinglecellrnaandbulkrnasequencingrevealedmalignantductalcellheterogeneityandprognosissignaturesinpancreaticcancer AT gaosi integrationofsinglecellrnaandbulkrnasequencingrevealedmalignantductalcellheterogeneityandprognosissignaturesinpancreaticcancer AT jiqingsi integrationofsinglecellrnaandbulkrnasequencingrevealedmalignantductalcellheterogeneityandprognosissignaturesinpancreaticcancer AT xuejiesong integrationofsinglecellrnaandbulkrnasequencingrevealedmalignantductalcellheterogeneityandprognosissignaturesinpancreaticcancer AT xuejiesong integrationofsinglecellrnaandbulkrnasequencingrevealedmalignantductalcellheterogeneityandprognosissignaturesinpancreaticcancer AT fuchunsi integrationofsinglecellrnaandbulkrnasequencingrevealedmalignantductalcellheterogeneityandprognosissignaturesinpancreaticcancer AT fuchunsi integrationofsinglecellrnaandbulkrnasequencingrevealedmalignantductalcellheterogeneityandprognosissignaturesinpancreaticcancer |