In-Depth Examination of TPBG as a New Predictive Indicator for Gastric Cancer

被引:0
作者
Yang, Lianlei [1 ]
Weng, Chunyan [2 ]
Zhang, Yaping [3 ]
Zhao, Yu [3 ]
Chen, Kexin [3 ]
Li, Guodong [3 ]
Zhong, Xueqing [3 ]
He, Chenghai [3 ]
机构
[1] First Peoples Hosp Linping Dist, Dept Gastroenterol, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Chinese Med Univ, Clin Med 1, Hangzhou, Zhejiang, Peoples R China
[3] Hangzhou Normal Univ, Affiliated Hosp, Dept Gastroenterol, Hangzhou, Zhejiang, Peoples R China
关键词
biomarker; gastric cancer; immune infiltration; PI3K/AKT signalling pathway; prognosis; TPBG; 5T4 ONCOFETAL ANTIGEN; EXPRESSION; TARGET; CELLS; GLYCOPROTEIN;
D O I
10.1111/jcmm.70354
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Trophoblast glycoprotein (TPBG) plays a significant part in the growth of specific cancers, yet its connection to gastric cancer (GC) remains uncertain. This research seeks to analyse the fluctuation in TPBG levels in GC and evaluate how TPBG expression relates to the prognosis of GC patients. TPBG expression in GC and normal gastric tissues was investigated in The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) database, further extracting the immunohistochemistry images from HPA database and validating by Western blot. The connection between TPBG and GC patients' survival rates was investigated by Kaplan-Meier and COX regression analysis. Genes related to TPBG were enriched using GO and KEGG data. In vitro and in vivo tumour models were utilised to evaluate the function of TPBG in GC. Western blot analysis was performed to detect the expression of PI3K/AKT signalling pathway proteins following TPBG knockdown. Immune infiltration was analysed using the CIBERSOFT and ssGSEA methods. The association between TPBG and immune cells that infiltrate tumours was evaluated through the utilisation of GSVA. TPBG expression increased in several tumour tissues (including GC) more than in adjacent noncancerous tissues. Elevated TPBG level predicted worse outcomes, such as poorer overall survival, pathological stage, and therapy response in GC. Enrichment analysis primarily focused on biological processes like the organisation of external encapsulating structures, extracellular structure, and collagen metabolism. Biological experiments further demonstrated that TPBG knockdown successfully inhibits the progression, migration, and invasion of GC cells. Western blot analysis revealed that TPBG knockdown inhibits the PI3K/AKT signalling pathway. Furthermore, TPBG is associated with the infiltration of immune cells in GC, which correlates with the expression of macrophage cells. There is a positive relationship between TPBG and malignant behaviour of GC tissues and cells, suggesting that TPBG can be useful for diagnosing and prognosing GC.
引用
收藏
页数:13
相关论文
共 25 条
  • [11] DKK1 Promotes Tumor Immune Evasion and Impedes Anti-PD-1 Treatment by Inducing Immunosuppressive Macrophages in Gastric Cancer
    Shi, Tao
    Zhang, Yipeng
    Wang, Yue
    Song, Xueru
    Wang, Hanbing
    Zhou, Xiaoyu
    Liang, Kaijie
    Luo, Yuting
    Che, Keying
    Wang, Xuan
    Pan, Yunfeng
    Liu, Fangcen
    Yang, Ju
    Liu, Qin
    Yu, Lixia
    Liu, Baorui
    Wei, Jia
    [J]. CANCER IMMUNOLOGY RESEARCH, 2022, 10 (12) : 1506 - 1524
  • [12] Smyth EC, 2020, LANCET, V396, P635, DOI 10.1016/S0140-6736(20)31288-5
  • [13] PROGNOSTIC-SIGNIFICANCE OF 5T4 ONCOFETAL ANTIGEN EXPRESSION IN COLORECTAL-CARCINOMA
    STARZYNSKA, T
    MARSH, PJ
    SCHOFIELD, PF
    ROBERTS, SA
    MYERS, KA
    STERN, PL
    [J]. BRITISH JOURNAL OF CANCER, 1994, 69 (05) : 899 - 902
  • [14] 5T4 oncofoetal antigen: an attractive target for immune intervention in cancer
    Stern, Peter L.
    Harrop, Richard
    [J]. CANCER IMMUNOLOGY IMMUNOTHERAPY, 2017, 66 (04) : 415 - 426
  • [15] Understanding and exploiting 5T4 oncofoetal glycoprotein expression
    Stern, Peter L.
    Brazzatti, Julie
    Sawan, Saladin
    McGinn, Owen J.
    [J]. SEMINARS IN CANCER BIOLOGY, 2014, 29 : 13 - 20
  • [16] Deciphering Innate Immune Cell-Tumor Microenvironment Crosstalk at a Single-Cell Level
    Sugimura, Ryohichi
    Chao, Yiming
    [J]. FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2022, 10
  • [17] Immune responses against shared antigens are common in esophago-gastric cancer and can be enhanced using CD40-activated B cells
    Thelen, Martin
    Keller, Diandra
    Lehmann, Jonas
    Wennhold, Kerstin
    Weitz, Hendrik
    Bauer, Eugen
    Gathof, Birgit
    Brueggemann, Monika
    Kotrova, Michaela
    Quaas, Alexander
    Mallmann, Christoph
    Chon, Seung-Hun
    Hillmer, Axel M.
    Bruns, Christiane
    von Bergwelt-Baildon, Michael
    Garcia-Marquez, Maria Alejandra
    Schloesser, Hans Anton
    [J]. JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2022, 10 (12)
  • [18] Tissue-based map of the human proteome
    Uhlen, Mathias
    Fagerberg, Linn
    Hallstroem, Bjoern M.
    Lindskog, Cecilia
    Oksvold, Per
    Mardinoglu, Adil
    Sivertsson, Asa
    Kampf, Caroline
    Sjoestedt, Evelina
    Asplund, Anna
    Olsson, IngMarie
    Edlund, Karolina
    Lundberg, Emma
    Navani, Sanjay
    Szigyarto, Cristina Al-Khalili
    Odeberg, Jacob
    Djureinovic, Dijana
    Takanen, Jenny Ottosson
    Hober, Sophia
    Alm, Tove
    Edqvist, Per-Henrik
    Berling, Holger
    Tegel, Hanna
    Mulder, Jan
    Rockberg, Johan
    Nilsson, Peter
    Schwenk, Jochen M.
    Hamsten, Marica
    von Feilitzen, Kalle
    Forsberg, Mattias
    Persson, Lukas
    Johansson, Fredric
    Zwahlen, Martin
    von Heijne, Gunnar
    Nielsen, Jens
    Ponten, Fredrik
    [J]. SCIENCE, 2015, 347 (6220)
  • [19] Trastuzumab Emtansine for Residual Invasive HER2-Positive Breast Cancer
    von Minckwitz, G.
    Huang, C. -S.
    Mano, M. S.
    Loibl, S.
    Mamounas, E. P.
    Untch, M.
    Wolmark, N.
    Rastogi, P.
    Schneeweiss, A.
    Redondo, A.
    Fischer, H. H.
    Jacot, W.
    Conlin, A. K.
    Arce-Salinas, C.
    Wapnir, I. L.
    Jackisch, C.
    DiGiovanna, M. P.
    Fasching, P. A.
    Crown, J. P.
    Wuelfing, P.
    Shao, Z.
    Caremoli, E. Rota
    Wu, H.
    Lam, L. H.
    Tesarowski, D.
    Smitt, M.
    Douthwaite, H.
    Singel, S. M.
    Geyer, C. E., Jr.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2019, 380 (07) : 617 - 628
  • [20] Wang RX, 2018, AM J CANCER RES, V8, P610