Page 33 - TD-3-1
P. 33

Tumor Discovery                                                       AI uncovers tumor spatial organization




                         A                                     B














                         C
















                         D                                   E













            Figure 3. The spatial clustering and downstream analysis results on human breast cancer from 10× Visium platform: (A) The ground truth of breast cancer
            data labeled by SEDR package; (B) the adjusted Rand index (ARI) values of seven compared methods on this spatial transcriptomics (ST) data; (C) the
            spatial domain identification results of DeepST, STAGATE, and VGAE_SGC on the breast cancer data; (D) the differential gene analysis between group 2
            or 11 and other clusters; and (E) the gene set enrichment analysis of differential genes in groups 2 and 11.

            specifically encompassing 15 cell types with 11,996 cells   approximation and projection (UMAP) plot illustrating
            and the same set of 313 genes (Figure 4A).         VGAE_SGC’s clustering results. Subsequently, we utilized
              We conducted a comparative analysis of the       the scanpy.tl.paga function within Scanpy to construct the
            clustering  accuracy  across the  seven  methods  using   spatial evolutionary trajectory, highlighting that group 0
            the aforementioned cropped ST data. Notably, VGAE_  represents regular cells and cluster 5 corresponds to tumor
            SGC and STAGATE exhibit proximity in performance,   cells in breast cancer.
            outperforming the remaining methods, as shown in     VGAE_SGC     excelled  in  discerning  cellular
            Figure 4B. Figure 4C portrays the spatial distribution of   compartmentalization and diverse cellular subpopulations
            spots in the VGAE_SGC case, revealing that clusters 0,   within spatial transcriptomic data. It also demonstrates
            1, 6, and 9 aligned with the annotated labels, as shown in   proficiency in detecting the tumor microenvironment,
            Figure 4A. In addition to conducting differential gene and   which is crucial for uncovering neo-cells, elucidating
            biological function analyses, we employed VGAE_SGC’s   carcinogenesis mechanisms, and advancing cancer
            clustering groups to infer the spatial development trajectory   treatments. However, it is essential to acknowledge the
            (Figure  4D). Initially, we present a uniform manifold   limitations of this approach. Notably, we did not leverage


            Volume 3 Issue 1 (2024)                         7                          https://doi.org/10.36922/td.2049
   28   29   30   31   32   33   34   35   36   37   38