{"id":2481,"date":"2014-05-02T00:00:00","date_gmt":"2014-05-02T07:00:00","guid":{"rendered":"https:\/\/vermont.salk.edu\/news-release\/ability-to-isolate-and-grow-breast-tissue-stem-cells-could-speed-cancer-research\/"},"modified":"2014-05-02T00:00:00","modified_gmt":"2014-05-02T07:00:00","slug":"ability-to-isolate-and-grow-breast-tissue-stem-cells-could-speed-cancer-research","status":"publish","type":"disclosure","link":"https:\/\/www.salk.edu\/es\/news-release\/ability-to-isolate-and-grow-breast-tissue-stem-cells-could-speed-cancer-research\/","title":{"rendered":"Ability to isolate and grow breast tissue stem cells could speed cancer research"},"content":{"rendered":"

\nLA JOLLA\u2014By carefully controlling the levels of two proteins, researchers at the Salk Institute have discovered how to keep mammary stem cells\u2014those that can form breast tissue\u2014alive and functioning in the lab. The new ability to propagate mammary stem cells is allowing them to study both breast development and the formation of breast cancers.\n<\/p>\n

\t“What we’ve shown is that we can take these cells out of a mouse and study them and regulate them in the laboratory by providing them with a specific factor,” says Peter C. Gray<\/a>, a staff scientist in Salk’s Laboratorios de la Fundaci\u00f3n Clayton para la Biolog\u00eda de los P\u00e9ptidos<\/a>, who collaborated on the new work with Benjamin T. Spike, a senior research associate in the laboratory of Salk Professor Geoffrey M. Wahl<\/a>.\n<\/p>\n

\"2025-CRIPTO-GRP78\"<\/p>\n

\nPeter C. Gray, Benjamin T. Spike and Geoffrey M. Wahl\n <\/p>\n

\nImagen: Cortes\u00eda del Instituto Salk de Estudios Biol\u00f3gicos\n<\/p>\n<\/div>\n

\tThe results of the study were published in the April 8th, 2014 issue of the journal Stem Cell Reports<\/em><\/a><\/em>.<\/p>\n

\nMammary stem cells can give rise to new breast cells during fetal development, adolescence or lactation and may also play a role in breast c\u00e1ncer<\/a>, so they represent a highly promising avenue for breast cancer research. But isolating the stem cells and maintaining them in the lab to study has been difficult. <\/p>\n

\n\t“There was a lot of prior work demonstrating that mammary-specific stem cells exist, but it was virtually impossible to isolate them in numbers from an adult,” says Spike. “But we previously found we could turn to early development, when the stem cells are present in higher proportions.”<\/p>\n

\n\tWhen the researchers used fetal breast tissue rather than adult tissue from mice, they were able to pinpoint which cells were stem cells but the cells would rapidly change when grown in a dish. A defining property of all stem cells is that when they divide into two new cells, they can form both stem cells and differentiated cells (cells on their way to becoming a specific type of tissue).<\/p>\n

\nSpike and Gray grew the mammary stem cells in culture dishes and stained them so that new stem cells appeared a different color from differentiated mammary cells. Then, they began testing the effects of two proteins\u2014known as CRIPTO and GRP78\u2014that play significant roles in both stem cell biology and embryonic development. <\/p>\n

\"2025-CRIPTO-GRP78\"<\/p>\n

\nWhen scientists add CRIPTO to a population of breast stem cells, they retain their ability to produce more stem cells, keeping the population constant. But when CRIPTO’s action is blocked with the molecule ALK4, the cells differentiate into mature cells and the population of stem cells shrinks.\n <\/p>\n

Haga clic aqu\u00ed<\/a> for a high resolution image.<\/p>\n

\nImage: Stem Cell Reports<\/em>, Spike, Benjamin T. et al. \/ Salk Institute for Biological Studies\n<\/p>\n<\/div>\n

\n\t“In normal conditions, we first see the cells as yellow\u2014the combination of red and green within a single cell\u2014then later see cells that are either red or green, showing that our cells had the capacity to make two different types of mature cells,” says Spike. “But then when we do the experiment again and start changing protein levels, the ratio of these cells becomes very different.”\n<\/p>\n

The researchers found that when they blocked CRIPTO, the cells mostly formed differentiated cells instead of new stem cells. Over time, this stem cell population shrank since they weren’t repopulating themselves. When they instead boosted levels of CRIPTO, the stem cell colony grew as new stem cells were produced more often than differentiated cells. <\/p>\n

\nIn studies in mice, the scientists also found that CRIPTO helped the animals form new mammary tissues, which led the team to hypothesize that CRIPTO may be produced by nearby cells in the fat to spur the growth of breast tissue.<\/p>\n

\nIn a previous study, Gray’s group had discovered that the protein GRP78 binds CRIPTO on the surface of cells and regulates CRIPTO function. This prompted the scientists to test whether GRP78 had an effect on the mammary stem cells. As they suspected, when cells lacked GRP78 on their surfaces, they didn’t respond to CRIPTO.\n<\/p>\n

Both CRIPTO and GRP78 have been implicated in cancers, including breast cancer and lung cancers. Scientists think high levels of either protein could encourage tumor growth using similar pathways that they use to spur breast tissue growth. With the new ability to isolate and sustain mammary stem cells, Spike and Gray hope they can uncover details on exactly what cellular programs CRIPTO and GRP78 activate. Understanding this in stem cells could further understanding on how these proteins are involved in tumor growth. <\/p>\n

\"2025-CRIPTO-GRP78\"<\/p>\n

\nIsolated fetal mammary cells show high levels of CRIPTO (green) and GRP78 (red), which have been found to help control the differentiation of mammary stem cells.\n <\/p>\n

\nImage: Stem Cell Reports<\/em>, Spike, Benjamin T. et al. \/ Salk Institute for Biological Studies\n<\/p>\n<\/div>\n

\nAdditionally the researchers think that targeting CRIPTO and GRP78\u2014which are ideal drug targets since they are present outside of cells\u2014could halt or slow cancer growth.
\n“It’s looking more and more like what’s required to target cancer is to have many therapeutics hitting different pathways,” says Gray. “We think targeting CRIPTO and GRP78 could be a unique way of supplementing existing treatment modalities by targeting stem cell-like cells in cancer.”\n<\/p>\n

\tOther researchers on the study were Evan Booker, Madhuri Kalathur, Rose Rodewald, Julia Lipianskaya, Justin La, Marielle He and Geoffrey M. Wahl of the Salk Institute for Biological Studies, and Jonathan A. Kelber, Tracy Wright and Richard Klemke of the University of California San Diego <\/p>\n

\n\tEste trabajo fue financiado por la Clayton Medical Research Foundation<\/a>, la Breast Cancer Research Foundation<\/a>, a Department of Defense award, a Cancer Center Core grant, and the Fundaci\u00f3n Ben\u00e9fica Leona M. y Harry B. Helmsley<\/a>.<\/p>\n

\nAcerca del Instituto Salk de Estudios Biol\u00f3gicos:<\/strong>
\nThe Salk Institute for Biological Studies is one of the world’s preeminent basic research institutions, where internationally renowned faculty probes fundamental life science questions in a unique, collaborative and creative environment. Focused both on discovery and on mentoring future generations of researchers, Salk scientists make groundbreaking contributions to our understanding of cancer, aging, Alzheimer’s, diabetes and infectious diseases by studying neuroscience, genetics, cell and plant biology, and related disciplines.\n<\/p>\n

\nLos logros del cuerpo docente han sido reconocidos con numerosos galardones, entre los que se incluyen premios Nobel y la pertenencia a la Academia Nacional de Ciencias. Fundado en 1960 por el Dr. Jonas Salk, pionero en la vacuna contra la poliomielitis, el Instituto es una organizaci\u00f3n independiente sin fines de lucro y un hito arquitect\u00f3nico.<\/p>","protected":false},"featured_media":0,"template":"","faculty":[90],"disease-research":[163,46],"class_list":["post-2481","disclosure","type-disclosure","status-publish","hentry","faculty-geoffrey-wahl","disease-research-breast-cancer","disease-research-cancer-biology"],"acf":[],"yoast_head":"\nAbility to isolate and grow breast tissue stem cells could speed cancer research - Salk Institute for Biological Studies<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.salk.edu\/es\/news-release\/ability-to-isolate-and-grow-breast-tissue-stem-cells-could-speed-cancer-research\/\" \/>\n<meta property=\"og:locale\" content=\"es_MX\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Ability to isolate and grow breast tissue stem cells could speed cancer research - Salk Institute for Biological Studies\" \/>\n<meta property=\"og:description\" content=\"LA JOLLA\u2014By carefully controlling the levels of two proteins, researchers at the Salk Institute have discovered how to keep mammary stem cells\u2014those that can form breast tissue\u2014alive and functioning in the lab. 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