<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(9)</volume><submitter>Mohammadnezhad L</submitter><pubmed_abstract>Primary Sjogren syndrome (pSS) is the second most common autoimmune disorder worldwide, which, in the worst scenario, progresses to Non-Hodgkin Lymphoma (NHL). Despite extensive studies, there is still a lack of knowledge about developing pSS for NHL. This study focused on cells' signaling in pSS progression to the NHL type of diffuse large B-cell lymphoma (DLBCL). Using bulk RNA and single cell analysis, we found five novel pathologic-independent clusters in DLBCL based on cells' signaling. B-cell receptor (BCR) signaling was identified as the only enriched signal in DLBCL and pSS peripheral naive B-cells or salivary gland-infiltrated cells. The evaluation of the genes in association with BCR has revealed that targeting &lt;i>CD79A&lt;/i>, &lt;i>CD79B&lt;/i>, and &lt;i>LAMTOR4&lt;/i> as the shared genes can provide novel biomarkers for pSS progression into lymphoma.</pubmed_abstract><journal>International journal of molecular sciences</journal><pagination>8385</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10179133</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>B-Cell Receptor Signaling Is Thought to Be a Bridge between Primary Sjogren Syndrome and Diffuse Large B-Cell Lymphoma.</pubmed_title><pmcid>PMC10179133</pmcid><pubmed_authors>Mohammadnezhad L</pubmed_authors><pubmed_authors>Dieli F</pubmed_authors><pubmed_authors>Guggino G</pubmed_authors><pubmed_authors>Shekarkar Azgomi M</pubmed_authors><pubmed_authors>Botta C</pubmed_authors><pubmed_authors>La Manna MP</pubmed_authors><pubmed_authors>Caccamo N</pubmed_authors></additional><is_claimable>false</is_claimable><name>B-Cell Receptor Signaling Is Thought to Be a Bridge between Primary Sjogren Syndrome and Diffuse Large B-Cell Lymphoma.</name><description>Primary Sjogren syndrome (pSS) is the second most common autoimmune disorder worldwide, which, in the worst scenario, progresses to Non-Hodgkin Lymphoma (NHL). Despite extensive studies, there is still a lack of knowledge about developing pSS for NHL. This study focused on cells' signaling in pSS progression to the NHL type of diffuse large B-cell lymphoma (DLBCL). Using bulk RNA and single cell analysis, we found five novel pathologic-independent clusters in DLBCL based on cells' signaling. B-cell receptor (BCR) signaling was identified as the only enriched signal in DLBCL and pSS peripheral naive B-cells or salivary gland-infiltrated cells. The evaluation of the genes in association with BCR has revealed that targeting &lt;i>CD79A&lt;/i>, &lt;i>CD79B&lt;/i>, and &lt;i>LAMTOR4&lt;/i> as the shared genes can provide novel biomarkers for pSS progression into lymphoma.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2024-11-21T05:38:12.166Z</modification><creation>2024-11-21T05:38:12.166Z</creation></dates><accession>S-EPMC10179133</accession><cross_references><pubmed>37176092</pubmed><doi>10.3390/ijms24098385</doi></cross_references></HashMap>