<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(1)</volume><submitter>Tang Y</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Ribosomal protein S6 (S6), a downstream effect media of the AKT/mTOR pathway, not only is a part of 40S small subunit of eukaryotic ribosome, but also involves in protein synthesis and cell proliferation during cancer development.&lt;h4>Methods&lt;/h4>In present study, we explore the association between phosphorylated S6 (p-S6) protein expression and clinicopathological features as well as prognostic implications in NSCLC. P-S6 was detected in tissue microarrays (TMAs) containing 350 NSCLC, 53 non-cancerous lung tissues (Non-CLT), and 88 cases of matched metastatic lymph node lesions via immunohistochemistry (IHC). Transwell assays and wound healing assay were used to assess the effects of p-S6 inhibition on NSCLC cell metastasis.&lt;h4>Results&lt;/h4>The p-S6 expression in NSCLC was more evident than that in Non-CLT (p &lt; 0.05). Compared to NSCLC patients who have no lymph node metastasis (LNM), those with LNM had higher p-S6 expression (p = 0.001). Regardless of lung squamous cell carcinoma (SCC) or adenocarcinoma (ADC), p-S6 was increased obviously in metastatic lymph nodes compared with matched primary cancers (p = 0.001, p = 0.022, respectively). Inhibition of p-S6 decreased the metastasis ability of NSCLC cells. In addition, p-S6 was an independent predicted marker for LNM in patients with NSCLC (p &lt; 0.001). According to survival analysis, patients with highly expressed p-S6 had a lower survival rate compared with that with lower expression (p = 0.013). P-S6 is an unfavorable independent prognostic factor for NSCLC patients (p = 0.011).&lt;h4>Conclusion&lt;/h4>Increased expression of p-S6 is not only a novel predictive biomarker of LNM but also poor prognosis in NSCLC.</pubmed_abstract><journal>BMC cancer</journal><pagination>564</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9123697</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Overexpressed p-S6 associates with lymph node metastasis and predicts poor prognosis in non-small cell lung cancer.</pubmed_title><pmcid>PMC9123697</pmcid><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Zheng H</pubmed_authors><pubmed_authors>Luo J</pubmed_authors><pubmed_authors>Zang H</pubmed_authors><pubmed_authors>Wen Q</pubmed_authors><pubmed_authors>Ma J</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors><pubmed_authors>Fan S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Overexpressed p-S6 associates with lymph node metastasis and predicts poor prognosis in non-small cell lung cancer.</name><description>&lt;h4>Background&lt;/h4>Ribosomal protein S6 (S6), a downstream effect media of the AKT/mTOR pathway, not only is a part of 40S small subunit of eukaryotic ribosome, but also involves in protein synthesis and cell proliferation during cancer development.&lt;h4>Methods&lt;/h4>In present study, we explore the association between phosphorylated S6 (p-S6) protein expression and clinicopathological features as well as prognostic implications in NSCLC. P-S6 was detected in tissue microarrays (TMAs) containing 350 NSCLC, 53 non-cancerous lung tissues (Non-CLT), and 88 cases of matched metastatic lymph node lesions via immunohistochemistry (IHC). Transwell assays and wound healing assay were used to assess the effects of p-S6 inhibition on NSCLC cell metastasis.&lt;h4>Results&lt;/h4>The p-S6 expression in NSCLC was more evident than that in Non-CLT (p &lt; 0.05). Compared to NSCLC patients who have no lymph node metastasis (LNM), those with LNM had higher p-S6 expression (p = 0.001). Regardless of lung squamous cell carcinoma (SCC) or adenocarcinoma (ADC), p-S6 was increased obviously in metastatic lymph nodes compared with matched primary cancers (p = 0.001, p = 0.022, respectively). Inhibition of p-S6 decreased the metastasis ability of NSCLC cells. In addition, p-S6 was an independent predicted marker for LNM in patients with NSCLC (p &lt; 0.001). According to survival analysis, patients with highly expressed p-S6 had a lower survival rate compared with that with lower expression (p = 0.013). P-S6 is an unfavorable independent prognostic factor for NSCLC patients (p = 0.011).&lt;h4>Conclusion&lt;/h4>Increased expression of p-S6 is not only a novel predictive biomarker of LNM but also poor prognosis in NSCLC.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2024-11-06T15:45:39.742Z</modification><creation>2024-11-06T15:45:39.742Z</creation></dates><accession>S-EPMC9123697</accession><cross_references><pubmed>35596155</pubmed><doi>10.1186/s12885-022-09664-4</doi></cross_references></HashMap>