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. 2020 Aug 3;8(8):267. doi: 10.3390/biomedicines8080267

Table 1.

Cargo molecules in EVs from various types of cells and effects of cargo molecules on pancreatic cancer cells (PCCs).

Cargo Source of EVs Type of Study Major Function of Cargo Molecules Ref.
miRNAs
miRNA-10a-5p CAFs isolated from human pancreatic cancer tissues In vitro Support the aggressiveness of PANC-1 and SW1990 cells [64]
miRNA-21 PSCs (human PSC21-S/T cell line), CAFs (human CAF-19 cell line) In vitro Reinforce the proliferation, migration and EMT process of PANC-1 and SUIT-2 cells; augment clonogenicity and sphere formation of Colo-357 cells [66,67]
miRNA-23b-3p PCCs (human PANC-1 cells) In vitro Increase the proliferation, migration and invasion of PANC-1 cells [11]
miRNA-106-5p CAFs isolated from human pancreatic cancer tissues In vitro Confer gemcitabine resistance in AsPC-1 cells [68]
miRNA-155 PCCs (gemcitabine-treated human MIAPaCa-2 and Colo-357 cells, gemcitabine-resistant human PANC-1 cells) In vitro, In vivo Inhibit gemcitabine-induced apoptosis in MIAPaCa-2 and Colo-357 cells in vitro; confer gemcitabine resistance in PANC-1 cells in vivo [15,16]
miRNA-194-5p Irradiated human PANC-1 and SW1990 cells In vitro, In vivo Augment the survival of SW1990 cells following radiation in vitro [20]
miRNA-210 CSCs derived from gemcitabine-resistant human BxPC-3 cells In vitro, In vivo Inhibit gemcitabine-induced apoptosis in BxPC-3 and PANC-1 cells in vitro; confer gemcitabine resistance in BxPC-3 cells in vivo [88]
miRNA-221 CAFs (human CAF-19 cell line), PSCs isolated from human pancreatic cancer tissues In vitro Stimulate the clonogenicity and sphere formation of Colo-357 cells [66]
miRNA-222 PCCs (human Hs 766 T-L3 cells) In vitro, In vivo Enhance the proliferation, migration and invasion of CAPAN-1 and Hs 766 T-L3 cells in vitro; promote cancer progression in vivo [12]
miRNA-365 TAMs (M2-polarized murine peritoneal macrophages) In vitro, In vivo Attenuate the gemcitabine efficacy in K989 murine cells [76]
miRNA-501-3p TAMs (M2-polarized human THP-1 cells) In vitro, In vivo Enhance the migration and invasion of PANC-1 and BxPC-3 cells in vitro; promote cancer growth and metastasis in vivo [80]
miRNA-5703 PSCs isolated from human pancreatic cancer tissues In vitro Promote the proliferation of Patu8988 and T3M4 cells [73]
Other non-coding RNAs
Circ-PDE8A PCCs (human Hs 766 T-L2 cells) In vitro, In vivo Facilitate the invasion of BxPC-3 and CAPAN-1 cells in vitro; enhance liver metastasis in vivo [24]
LncRNA-HULC PCCs (human PANC-1 cells) In vitro, In vivo Trigger migration, invasion and EMT process in PANC-1 and MIAPaCa-2 cells in vitro; promote cancer progression in vivo [30]
LncRNA-SBF2-AS1 TAMs (M2-polarized human THP-1 cells) In vitro, In vivo Enhance the proliferation, migration and invasion of PANC-1 cells in vitro; force the tumorigenic ability of PANC-1 cells in vivo [81]
LncRNA-SOX2OT PCCs (human Hs 766 T and Hs 766 T-L2 cells) In vitro, In vivo Promote EMT and stemness in Hs 766 T cells in vitro; trigger EMT, stemness and metastasis in vivo [33]
mRNAs
CAT and SOD2 PCCs (gemcitabine-treated human MIAPaCa-2 and Colo-357 cells) In vitro Protect cell death induced by ROS in gemcitabine-treated MIAPaCa-2 cells [16]
SNAI1 CAFs isolated from human pancreatic cancer tissues In vitro Promote the proliferation and gemcitabine resistance in AsPC-1 cells [75]
Proteins
AEP PCCs (human BxPC-3 cells) In vitro Aggravate the invasion ability of BxPC-3 and AsPC-1 cells [38]
ANXA1 PCCs (human MIAPaCa-2 cells) In vitro Facilitate the EMT, migration and invasion in MIAPaCa-2 cells [43]
EphA2 PCCs (gemcitabine-resistant human PANC-1 cells) In vitro Develop gemcitabine resistance in MIAPaCa-2 and BxPC-3 cells [48]
Lin28B PCCs (human PANC-1 and MIAPaCa-2 cells) In vitro, In vivo Increase the levels of PDGF in PANC-1 and MIAPaCa-2 cells, ultimately enhancing PSCs recruitment to the metastatic site [52]
ZIP4 PCCs (hamster PC-1.0 cells) In vitro, In vivo Promote the proliferation and migration of PC-1.0 cells in vitro; enhance the growth of cancer in vivo [59]

Abbreviations: AEP: Asparaginyl endopeptidase; ANXA1: Annexin A1; CAFs: Cancer-associated fibroblasts; CAT: Catalase; CSCs: Cancer stem cells; EMT: Epithelial-mesenchymal transition; EphA2: Ephrin type-A receptor 2; EVs: Extracellular vesicles; Lin28B: Lin-28 homolog B; MiRNA: MicroRNA; PDGF: Platelet-derived growth factor; PSCs: Pancreatic stellate cells; ROS: Reactive oxygen species; SNAI1: Snail family transcriptional repressor 1; SOD2: Superoxide dismutase 2; TAMs: Tumor-associated macrophages; ZIP4: Zrt- and Irt-like protein 4.