<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(58)</volume><submitter>Chen H</submitter><pubmed_abstract>Kallikrein-related peptidase 6 (KLK6) overexpression is commonly observed in primary tumors of colorectal cancer (CRC) patients and has been associated with tumor aggressiveness, metastasis, and poor prognosis. We previously established a unique contribution of KLK6 in colon cancer metastasis via a specific network of microRNAs and mRNAs. Here we evaluated the cellular functions of KLK6 protease in Caco-2 colon adenocarcinoma cell line after introduction of the enzymatically active or inactive form of the enzyme. We found that proteolytically active KLK6 increased Caco-2 cells invasiveness in vitro and decreased the animal survival in the orthotopic colon cancer model. The active KLK6 induced phosphorylation of SMAD 2/3 proteins leading to the altered expression of the epithelial-mesenchymal transition (EMT) markers. KLK6 overexpression also induced the RNA-binding protein LIN28B and high-mobility group AT-hook 2 (HMGA2) transcription factor, two essential regulators of cell invasion and metastasis. In the CRC patients, KLK6 protein levels were elevated in the non-cancerous distant and adjacent tissues, compared to their paired tumor tissues (p &lt; 0.0001 and p = 0.0157, respectively). Patients with mutant K-RAS tumors had significantly higher level of KLK6 protein in the luminal surface of non-cancerous distant tissue, compared to the corresponding tissues of the patients with K-RAS wild type tumors (p ≤ 0.05). Furthermore, KLK6 and HMGA2 immunohistochemistry (IHC) scores in patients' tumors and paired adjacent tissues positively correlated (Spearman correlation P &lt; 0.01 and p = 0.03, respectively). These findings demonstrate the critical function of the KLK6 enzyme in colon cancer progression and its contribution to the signaling network in colon cancer.</pubmed_abstract><journal>Oncotarget</journal><pagination>6062-6078</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6817440</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Kallikrein 6 protease advances colon tumorigenesis via induction of the high mobility group A2 protein.</pubmed_title><pmcid>PMC6817440</pmcid><pubmed_authors>Ignatenko NA</pubmed_authors><pubmed_authors>Krouse RS</pubmed_authors><pubmed_authors>Sells E</pubmed_authors><pubmed_authors>Pampalakis G</pubmed_authors><pubmed_authors>Nagle RB</pubmed_authors><pubmed_authors>Sotiropoulou G</pubmed_authors><pubmed_authors>Abril ER</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Hsu CH</pubmed_authors><pubmed_authors>Pandey R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Kallikrein 6 protease advances colon tumorigenesis via induction of the high mobility group A2 protein.</name><description>Kallikrein-related peptidase 6 (KLK6) overexpression is commonly observed in primary tumors of colorectal cancer (CRC) patients and has been associated with tumor aggressiveness, metastasis, and poor prognosis. We previously established a unique contribution of KLK6 in colon cancer metastasis via a specific network of microRNAs and mRNAs. Here we evaluated the cellular functions of KLK6 protease in Caco-2 colon adenocarcinoma cell line after introduction of the enzymatically active or inactive form of the enzyme. We found that proteolytically active KLK6 increased Caco-2 cells invasiveness in vitro and decreased the animal survival in the orthotopic colon cancer model. The active KLK6 induced phosphorylation of SMAD 2/3 proteins leading to the altered expression of the epithelial-mesenchymal transition (EMT) markers. KLK6 overexpression also induced the RNA-binding protein LIN28B and high-mobility group AT-hook 2 (HMGA2) transcription factor, two essential regulators of cell invasion and metastasis. In the CRC patients, KLK6 protein levels were elevated in the non-cancerous distant and adjacent tissues, compared to their paired tumor tissues (p &lt; 0.0001 and p = 0.0157, respectively). Patients with mutant K-RAS tumors had significantly higher level of KLK6 protein in the luminal surface of non-cancerous distant tissue, compared to the corresponding tissues of the patients with K-RAS wild type tumors (p ≤ 0.05). Furthermore, KLK6 and HMGA2 immunohistochemistry (IHC) scores in patients' tumors and paired adjacent tissues positively correlated (Spearman correlation P &lt; 0.01 and p = 0.03, respectively). These findings demonstrate the critical function of the KLK6 enzyme in colon cancer progression and its contribution to the signaling network in colon cancer.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Oct</publication><modification>2024-11-15T12:57:59.592Z</modification><creation>2019-11-12T08:05:10Z</creation></dates><accession>S-EPMC6817440</accession><cross_references><pubmed>31692974</pubmed><doi>10.18632/oncotarget.27153</doi></cross_references></HashMap>